Canonical Allele Identifier: CA359786871
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882064T>A , CM000667.2:g.56882064T>A GRCh38
NC_000005.9:g.56177891T>A , CM000667.1:g.56177891T>A GRCh37
NC_000005.8:g.56213648T>A NCBI36
NG_031884.1:g.71992T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2864T>A MANE Select ENSP00000382423.3:p.Met955Lys
ENST00000399503.3:c.2864T>A ENSP00000382423.3:p.Met955Lys
NM_005921.1:c.2864T>A NP_005912.1:p.Met955Lys
XM_005248519.3:c.2486T>A XP_005248576.2:p.Met829Lys
XM_011543406.1:c.2609T>A XP_011541708.1:p.Met870Lys
XM_011543407.1:c.2585T>A XP_011541709.1:p.Met862Lys
XM_011543408.1:c.2864T>A XP_011541710.1:p.Met955Lys
XM_017009484.1:c.2453T>A XP_016864973.1:p.Met818Lys
XM_017009485.1:c.2375T>A XP_016864974.1:p.Met792Lys
XR_001742068.2:n.2895T>A
NM_005921.2:c.2864T>A MANE Select NP_005912.1:p.Met955Lys