Canonical Allele Identifier: CA359781393
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875285T>C , CM000667.2:g.56875285T>C GRCh38
NC_000005.9:g.56171112T>C , CM000667.1:g.56171112T>C GRCh37
NC_000005.8:g.56206869T>C NCBI36
NG_031884.1:g.65213T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1940T>C MANE Select ENSP00000382423.3:p.Val647Ala
ENST00000399503.3:c.1940T>C ENSP00000382423.3:p.Val647Ala
NM_005921.1:c.1940T>C NP_005912.1:p.Val647Ala
XM_005248519.3:c.1562T>C XP_005248576.2:p.Val521Ala
XM_011543406.1:c.1685T>C XP_011541708.1:p.Val562Ala
XM_011543407.1:c.1686+2280T>C XP_011541709.1:n.1686+2280T>C
XM_011543408.1:c.1940T>C XP_011541710.1:p.Val647Ala
XM_017009484.1:c.1529T>C XP_016864973.1:p.Val510Ala
XM_017009485.1:c.1451T>C XP_016864974.1:p.Val484Ala
XR_001742068.2:n.1971T>C
NM_005921.2:c.1940T>C MANE Select NP_005912.1:p.Val647Ala