Canonical Allele Identifier: CA359802489
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859799G>T , CM000667.2:g.56859799G>T GRCh38
NC_000005.9:g.56155626G>T , CM000667.1:g.56155626G>T GRCh37
NC_000005.8:g.56191383G>T NCBI36
NG_031884.1:g.49727G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.718G>T MANE Select ENSP00000382423.3:p.Ala240Ser
ENST00000399503.3:c.718G>T ENSP00000382423.3:p.Ala240Ser
NM_005921.1:c.718G>T NP_005912.1:p.Ala240Ser
XM_005248519.3:c.340G>T XP_005248576.2:p.Ala114Ser
XM_011543406.1:c.463G>T XP_011541708.1:p.Ala155Ser
XM_011543407.1:c.718G>T XP_011541709.1:p.Ala240Ser
XM_011543408.1:c.718G>T XP_011541710.1:p.Ala240Ser
XM_017009484.1:c.307G>T XP_016864973.1:p.Ala103Ser
XM_017009485.1:c.229G>T XP_016864974.1:p.Ala77Ser
XR_001742068.2:n.749G>T
NM_005921.2:c.718G>T MANE Select NP_005912.1:p.Ala240Ser