Canonical Allele Identifier: CA392929318
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435145G>T , CM000677.2:g.66435145G>T GRCh38
NC_000015.9:g.66727483G>T , CM000677.1:g.66727483G>T GRCh37
NC_000015.8:g.64514537G>T NCBI36
NG_008305.1:g.53273G>T , LRG_725:g.53273G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307102.10:c.199G>T MANE Select ENSP00000302486.5:p.Asp67Tyr
ENST00000307102.9:c.199G>T ENSP00000302486.4:p.Asp67Tyr
ENST00000425818.2:n.710G>T
NM_002755.3:c.199G>T , LRG_725t1:c.199G>T NP_002746.1:p.Asp67Tyr
XM_011521783.1:c.133G>T XP_011520085.1:p.Asp45Tyr
XM_011521783.3:c.133G>T XP_011520085.1:p.Asp45Tyr
XM_017022411.2:c.199G>T XP_016877900.1:p.Asp67Tyr
XM_017022412.1:c.133G>T XP_016877901.1:p.Asp45Tyr
NM_002755.4:c.199G>T MANE Select NP_002746.1:p.Asp67Tyr