Linked Data
ClinVar Variation Id:
418295
ClinVar RCV Id:
RCV000480079
RCV000505013
RCV000505174
RCV000504782
RCV000805545
RCV001542748
RCV002313243
RCV001805096
dbSNP Id:
rs559155109
ExAC:
4:128841981 A / G
gnomAD v2:
4-128841981-A-G
gnomAD v3:
4-127920826-A-G
gnomAD v4:
4-127920826-A-G
COSMIC:
COSM1215009
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127920826A>G , CM000666.2:g.127920826A>G | GRCh38 |
| NC_000004.11:g.128841981A>G , CM000666.1:g.128841981A>G | GRCh37 |
| NC_000004.10:g.129061431A>G | NCBI36 |
| NG_008657.1:g.50159T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.1361T>C | ENSP00000296468.3:p.Met454Thr | |
| ENST00000509826.2:c.*682T>C | ENSP00000421176.2:n.*682T>C | |
| ENST00000513559.6:c.1079T>C | ENSP00000425000.2:p.Met360Thr | |
| ENST00000515130.6:c.*246T>C | ENSP00000493056.1:n.*246T>C | |
| ENST00000641025.1:c.*246T>C | ENSP00000493346.1:n.*246T>C | |
| ENST00000641092.1:c.*246T>C | ENSP00000493392.1:n.*246T>C | |
| ENST00000641133.1:c.*1362T>C | ENSP00000493192.1:n.*1362T>C | |
| ENST00000641146.1:n.1914T>C | ||
| ENST00000641147.1:c.911T>C | ENSP00000493133.1:p.Met304Thr | |
| ENST00000641178.1:c.1226T>C | ENSP00000492989.1:p.Met409Thr | |
| ENST00000641186.1:c.1247T>C | ENSP00000493347.1:p.Met416Thr | |
| ENST00000641228.1:c.*933T>C | ENSP00000493194.1:n.*933T>C | |
| ENST00000641332.1:c.*503T>C | ENSP00000493397.1:n.*503T>C | |
| ENST00000641340.1:c.*1177T>C | ENSP00000493191.1:n.*1177T>C | |
| ENST00000641388.1:n.608T>C | ||
| ENST00000641393.1:c.911T>C | ENSP00000493197.1:p.Met304Thr | |
| ENST00000641397.1:c.*246T>C | ENSP00000493406.1:n.*246T>C | |
| ENST00000641413.1:c.286T>C | ||
| ENST00000641434.1:c.1361T>C | ENSP00000493279.1:p.Met454Thr | |
| ENST00000641464.1:c.*594T>C | ENSP00000493438.1:n.*594T>C | |
| ENST00000641482.1:c.*933T>C | ENSP00000493277.1:n.*933T>C | |
| ENST00000641508.1:c.*594T>C | ENSP00000493209.1:n.*594T>C | |
| ENST00000641509.1:c.1046T>C | ENSP00000493459.1:p.Met349Thr | |
| ENST00000641590.1:c.*933T>C | ENSP00000493132.1:n.*933T>C | |
| ENST00000641658.1:c.*526T>C | ENSP00000492987.1:n.*526T>C | |
| ENST00000641686.2:c.1361T>C MANE Select | ENSP00000493218.2:p.Met454Thr | |
| ENST00000641690.1:c.1160T>C | ENSP00000492966.1:p.Met387Thr | |
| ENST00000641742.1:c.*526T>C | ENSP00000493315.1:n.*526T>C | |
| ENST00000641748.1:c.1361T>C | ENSP00000493330.1:p.Met454Thr | |
| ENST00000641753.1:c.1188T>C | ||
| ENST00000641774.1:c.*613T>C | ENSP00000492960.1:n.*613T>C | |
| ENST00000641843.1:c.*422T>C | ENSP00000493174.1:n.*422T>C | |
| ENST00000641869.1:c.562T>C | ||
| ENST00000641870.1:c.*1109T>C | ENSP00000493044.1:n.*1109T>C | |
| ENST00000641882.1:c.*526T>C | ENSP00000493301.1:n.*526T>C | |
| ENST00000641928.1:c.*490T>C | ENSP00000493418.1:n.*490T>C | |
| ENST00000641949.1:c.564T>C | ENSP00000492891.1:p.His188= | |
| ENST00000642012.1:n.1225T>C | ||
| ENST00000642034.1:c.*246T>C | ENSP00000493285.1:n.*246T>C | |
| ENST00000642042.1:c.*680T>C | ENSP00000493260.1:n.*680T>C | |
| ENST00000642078.1:c.*422T>C | ENSP00000492885.1:n.*422T>C | |
| ENST00000296468.7:c.1361T>C | ENSP00000296468.3:p.Met454Thr | |
| ENST00000513559.5:c.1226T>C | ENSP00000425000.1:p.Met409Thr | |
| ENST00000515130.5:n.1703T>C | ||
| NM_152778.2:c.1361T>C | NP_689991.1:p.Met454Thr | |
| XM_005262893.1:c.1361T>C | XP_005262950.1:p.Met454Thr | |
| XM_005262896.1:c.1214T>C | XP_005262953.1:p.Met405Thr | |
| XM_005262897.1:c.1160T>C | XP_005262954.1:p.Met387Thr | |
| XM_005262898.2:c.*933T>C | XP_005262955.1:n.*933T>C | |
| XM_011531830.1:c.1247T>C | XP_011530132.1:p.Met416Thr | |
| XM_011531831.1:c.1046T>C | XP_011530133.1:p.Met349Thr | |
| XM_011531832.1:c.*933T>C | XP_011530134.1:n.*933T>C | |
| XR_938717.1:n.1844T>C | ||
| NM_001363520.1:c.1160T>C | NP_001350449.1:p.Met387Thr | |
| NM_001363521.1:c.1046T>C | NP_001350450.1:p.Met349Thr | |
| XM_005262898.3:c.*933T>C | XP_005262955.1:n.*933T>C | |
| XM_017007989.1:c.*933T>C | XP_016863478.1:n.*933T>C | |
| XM_024453981.1:c.1226T>C | XP_024309749.1:p.Met409Thr | |
| XM_024453982.1:c.1112T>C | XP_024309750.1:p.Met371Thr | |
| XM_024453983.1:c.911T>C | XP_024309751.1:p.Met304Thr | |
| XR_001741194.1:n.1334T>C | ||
| XR_001741195.1:n.1220T>C | ||
| XR_001741196.1:n.1133T>C | ||
| XR_001741197.1:n.1980T>C | ||
| XR_001741198.2:n.1876T>C | ||
| XR_001741199.1:n.1189T>C | ||
| XR_938717.2:n.1844T>C | ||
| NM_001363520.2:c.1160T>C | NP_001350449.1:p.Met387Thr | |
| NM_001363521.2:c.1046T>C | NP_001350450.1:p.Met349Thr | |
| NM_001371590.1:c.1226T>C | NP_001358519.1:p.Met409Thr | |
| NM_001371591.1:c.1370T>C | NP_001358520.1:p.Met457Thr | |
| NM_001371592.1:c.1367T>C | NP_001358521.1:p.Met456Thr | |
| NM_001371593.1:c.1247T>C | NP_001358522.1:p.Met416Thr | |
| NM_001371594.1:c.1214T>C | NP_001358523.1:p.Met405Thr | |
| NM_001371595.1:c.1079T>C | NP_001358524.1:p.Met360Thr | |
| NM_001371596.2:c.1361T>C MANE Select | NP_001358525.1:p.Met454Thr | |
| NM_152778.3:c.1361T>C | NP_689991.1:p.Met454Thr | |
| NM_152778.4:c.1361T>C | NP_689991.1:p.Met454Thr |