Canonical Allele Identifier: CA444391740

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155685T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859858T>A , CM000667.2:g.56859858T>A	GRCh38
NC_000005.9:g.56155685T>A , CM000667.1:g.56155685T>A	GRCh37
NC_000005.8:g.56191442T>A	NCBI36
NG_031884.1:g.49786T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.777T>A MANE Select	ENSP00000382423.3:p.Gly259=
ENST00000399503.3:c.777T>A	ENSP00000382423.3:p.Gly259=
NM_005921.1:c.777T>A	NP_005912.1:p.Gly259=
XM_005248519.3:c.399T>A	XP_005248576.2:p.Gly133=
XM_011543406.1:c.522T>A	XP_011541708.1:p.Gly174=
XM_011543407.1:c.777T>A	XP_011541709.1:p.Gly259=
XM_011543408.1:c.777T>A	XP_011541710.1:p.Gly259=
XM_017009484.1:c.366T>A	XP_016864973.1:p.Gly122=
XM_017009485.1:c.288T>A	XP_016864974.1:p.Gly96=
XR_001742068.2:n.808T>A
NM_005921.2:c.777T>A MANE Select	NP_005912.1:p.Gly259=