UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152139955G>T , CM000668.2:g.152139955G>T | GRCh38 |
| NC_000006.11:g.152461090G>T , CM000668.1:g.152461090G>T | GRCh37 |
| NC_000006.10:g.152502783G>T | NCBI36 |
| NG_012855.1:g.502445C>A | |
| NG_012855.2:g.502445C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354674.5:c.1987C>A MANE Plus Clinical | ENSP00000346701.4:p.Leu663Ile | |
| ENST00000367255.10:c.25453C>A MANE Select | ENSP00000356224.5:p.Leu8485Ile | |
| ENST00000423061.6:c.25309C>A | ENSP00000396024.1:p.Leu8437Ile | |
| ENST00000672154.1:c.855C>A | ||
| ENST00000672169.1:c.1188C>A | ||
| ENST00000673173.1:c.1097C>A | ||
| ENST00000673451.1:c.1225C>A | ENSP00000500189.1:p.Leu409Ile | |
| ENST00000341594.9:c.24238C>A | ENSP00000341887.6:p.Leu8080Ile | |
| ENST00000347037.9:n.2201C>A | ||
| ENST00000354674.4:c.1987C>A | ENSP00000346701.4:p.Leu663Ile | |
| ENST00000367251.7:c.4288C>A | ENSP00000356220.3:p.Leu1430Ile | |
| ENST00000367255.9:c.25453C>A | ENSP00000356224.5:p.Leu8485Ile | |
| ENST00000367256.9:n.9145C>A | ||
| ENST00000367257.8:c.3391C>A | ENSP00000356226.4:p.Leu1131Ile | |
| ENST00000409694.6:n.9037C>A | ||
| ENST00000423061.5:c.25309C>A | ENSP00000396024.1:p.Leu8437Ile | |
| ENST00000460912.6:n.2067C>A | ||
| ENST00000478916.5:n.4475C>A | ||
| ENST00000536990.5:n.2290C>A | ||
| ENST00000539504.5:c.1918C>A | ENSP00000441052.1:p.Leu640Ile | |
| NM_033071.3:c.25309C>A | NP_149062.1:p.Leu8437Ile | |
| NM_182961.3:c.25453C>A | NP_892006.3:p.Leu8485Ile | |
| XM_006715407.1:c.25558C>A | XP_006715470.1:p.Leu8520Ile | |
| XM_006715408.1:c.25546C>A | XP_006715471.1:p.Leu8516Ile | |
| XM_006715409.1:c.25537C>A | XP_006715472.1:p.Leu8513Ile | |
| XM_006715410.1:c.25558C>A | XP_006715473.1:p.Leu8520Ile | |
| XM_006715411.1:c.25507C>A | XP_006715474.1:p.Leu8503Ile | |
| XM_006715412.1:c.25543C>A | XP_006715475.1:p.Leu8515Ile | |
| XM_006715413.1:c.25489C>A | XP_006715476.1:p.Leu8497Ile | |
| XM_006715414.1:c.25486C>A | XP_006715477.1:p.Leu8496Ile | |
| XM_006715415.1:c.25489C>A | XP_006715478.1:p.Leu8497Ile | |
| XM_006715416.1:c.25474C>A | XP_006715479.1:p.Leu8492Ile | |
| XM_006715417.1:c.25417C>A | XP_006715480.1:p.Leu8473Ile | |
| XM_006715420.1:c.25405C>A | XP_006715483.1:p.Leu8469Ile | |
| XM_006715421.1:c.25402C>A | XP_006715484.1:p.Leu8468Ile | |
| XM_006715422.1:c.25399C>A | XP_006715485.1:p.Leu8467Ile | |
| XM_006715423.1:c.25558C>A | XP_006715486.1:p.Leu8520Ile | |
| XM_006715424.1:c.25558C>A | XP_006715487.1:p.Leu8520Ile | |
| XM_006715425.1:c.25489C>A | XP_006715488.1:p.Leu8497Ile | |
| XM_011535641.1:c.25555C>A | XP_011533943.1:p.Leu8519Ile | |
| XM_011535642.1:c.25543C>A | XP_011533944.1:p.Leu8515Ile | |
| XM_011535643.1:c.25393C>A | XP_011533945.1:p.Leu8465Ile | |
| XM_011535644.1:c.23833C>A | XP_011533946.1:p.Leu7945Ile | |
| XM_011535645.1:c.23326C>A | XP_011533947.1:p.Leu7776Ile | |
| XM_011535647.1:c.18793C>A | XP_011533949.1:p.Leu6265Ile | |
| NM_001347701.1:c.2059C>A | NP_001334630.1:p.Leu687Ile | |
| NM_001347702.1:c.1987C>A | NP_001334631.1:p.Leu663Ile | |
| XM_006715408.2:c.25546C>A | XP_006715471.1:p.Leu8516Ile | |
| XM_006715410.2:c.25558C>A | XP_006715473.1:p.Leu8520Ile | |
| XM_006715412.2:c.25543C>A | XP_006715475.1:p.Leu8515Ile | |
| XM_006715413.2:c.25489C>A | XP_006715476.1:p.Leu8497Ile | |
| XM_006715415.2:c.25489C>A | XP_006715478.1:p.Leu8497Ile | |
| XM_006715416.2:c.25474C>A | XP_006715479.1:p.Leu8492Ile | |
| XM_006715417.2:c.25417C>A | XP_006715480.1:p.Leu8473Ile | |
| XM_006715420.2:c.25405C>A | XP_006715483.1:p.Leu8469Ile | |
| XM_006715421.2:c.25402C>A | XP_006715484.1:p.Leu8468Ile | |
| XM_006715423.2:c.25558C>A | XP_006715486.1:p.Leu8520Ile | |
| XM_006715424.2:c.25558C>A | XP_006715487.1:p.Leu8520Ile | |
| XM_006715425.2:c.25489C>A | XP_006715488.1:p.Leu8497Ile | |
| XM_011535641.2:c.25555C>A | XP_011533943.1:p.Leu8519Ile | |
| XM_011535642.2:c.25543C>A | XP_011533944.1:p.Leu8515Ile | |
| XM_011535645.2:c.23326C>A | XP_011533947.1:p.Leu7776Ile | |
| XM_017010608.1:c.25558C>A | XP_016866097.1:p.Leu8520Ile | |
| XM_017010609.1:c.25558C>A | XP_016866098.1:p.Leu8520Ile | |
| XM_017010610.1:c.25537C>A | XP_016866099.1:p.Leu8513Ile | |
| XM_017010611.2:c.25531C>A | XP_016866100.1:p.Leu8511Ile | |
| XM_017010612.1:c.25480C>A | XP_016866101.1:p.Leu8494Ile | |
| XM_017010613.1:c.25486C>A | XP_016866102.1:p.Leu8496Ile | |
| XM_017010614.1:c.25402C>A | XP_016866103.1:p.Leu8468Ile | |
| XM_017010615.1:c.25333C>A | XP_016866104.1:p.Leu8445Ile | |
| XM_017010616.1:c.25489C>A | XP_016866105.1:p.Leu8497Ile | |
| XM_017010617.1:c.25486C>A | XP_016866106.1:p.Leu8496Ile | |
| XM_017010618.1:c.25474C>A | XP_016866107.1:p.Leu8492Ile | |
| XM_017010619.1:c.23833C>A | XP_016866108.1:p.Leu7945Ile | |
| NM_182961.4:c.25453C>A MANE Select | NP_892006.3:p.Leu8485Ile | |
| NM_001347701.2:c.2059C>A | NP_001334630.1:p.Leu687Ile | |
| NM_001347702.2:c.1987C>A MANE Plus Clinical | NP_001334631.1:p.Leu663Ile | |
| NM_033071.5:c.25309C>A | NP_149062.2:p.Leu8437Ile |