Linked Data
ClinVar Variation Id:
2848760
ClinVar RCV Id:
RCV003655968
MyVariant Identifiers:
chr15:g.66782911C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66490573C>A , CM000677.2:g.66490573C>A | GRCh38 |
| NC_000015.9:g.66782911C>A , CM000677.1:g.66782911C>A | GRCh37 |
| NC_000015.8:g.64569965C>A | NCBI36 |
| NG_008305.1:g.108701C>A , LRG_725:g.108701C>A | |
| NG_051234.1:g.12243G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684779.1:c.*188C>A (MAP2K1) | ENSP00000508681.1:n.*188C>A | |
| ENST00000685172.1:c.1094C>A (MAP2K1) | ENSP00000509604.1:p.Ala365Asp | |
| ENST00000685763.1:c.993C>A (MAP2K1) | ENSP00000509016.1:p.Gly331= | |
| ENST00000686347.1:c.813C>A (MAP2K1) | ENSP00000509027.1:p.Gly271= | |
| ENST00000687191.1:n.3420C>A (MAP2K1) | ||
| ENST00000687481.1:n.555C>A (MAP2K1) | ||
| ENST00000688689.1:n.895C>A (MAP2K1) | ||
| ENST00000689951.1:c.1191C>A (MAP2K1) | ENSP00000509308.1:p.Gly397= | |
| ENST00000691077.1:c.*2299C>A (MAP2K1) | ENSP00000509843.1:n.*2299C>A | |
| ENST00000691576.1:c.1011C>A (MAP2K1) | ENSP00000510066.1:p.Gly337= | |
| ENST00000691937.1:c.*121C>A (MAP2K1) | ENSP00000508768.1:n.*121C>A | |
| ENST00000692487.1:c.*2740C>A (MAP2K1) | ENSP00000509534.1:n.*2740C>A | |
| ENST00000692683.1:c.1074C>A (MAP2K1) | ENSP00000508437.1:p.Gly358= | |
| ENST00000693150.1:c.996C>A (MAP2K1) | ENSP00000510309.1:p.Gly332= | |
| ENST00000307102.10:c.1140C>A (MAP2K1) MANE Select | ENSP00000302486.5:p.Gly380= | |
| ENST00000307102.9:c.1140C>A (MAP2K1) | ENSP00000302486.4:p.Gly380= | |
| ENST00000395589.6:c.*166G>T (SNAPC5) | ENSP00000378954.2:n.*166G>T | |
| ENST00000563480.6:c.*166G>T (SNAPC5) | ENSP00000457892.1:n.*166G>T | |
| ENST00000566326.1:c.612C>A (MAP2K1) | ENSP00000456438.1:p.Gly204= | |
| NM_002755.3:c.1140C>A , LRG_725t1:c.1140C>A (MAP2K1) | NP_002746.1:p.Gly380= | |
| NM_006049.2:c.*166G>T (SNAPC5) | NP_006040.1:n.*166G>T | |
| XM_011521783.1:c.1074C>A (MAP2K1) | XP_011520085.1:p.Gly358= | |
| NM_006049.3:c.*166G>T (SNAPC5) | NP_006040.1:n.*166G>T | |
| NR_138061.1:n.685G>T (SNAPC5) | ||
| XM_011521783.3:c.1074C>A (MAP2K1) | XP_011520085.1:p.Gly358= | |
| XM_017022411.2:c.1062C>A (MAP2K1) | XP_016877900.1:p.Gly354= | |
| XM_017022412.1:c.996C>A (MAP2K1) | XP_016877901.1:p.Gly332= | |
| XM_017022413.1:c.612C>A (MAP2K1) | XP_016877902.1:p.Gly204= | |
| NM_002755.4:c.1140C>A (MAP2K1) MANE Select | NP_002746.1:p.Gly380= | |
| NM_006049.4:c.*166G>T (SNAPC5) | NP_006040.1:n.*166G>T | |
| NR_138061.2:n.632G>T (SNAPC5) |