Canonical Allele Identifier: CA444391656

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155604T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859777T>A , CM000667.2:g.56859777T>A	GRCh38
NC_000005.9:g.56155604T>A , CM000667.1:g.56155604T>A	GRCh37
NC_000005.8:g.56191361T>A	NCBI36
NG_031884.1:g.49705T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.696T>A MANE Select	ENSP00000382423.3:p.Ser232=
ENST00000399503.3:c.696T>A	ENSP00000382423.3:p.Ser232=
NM_005921.1:c.696T>A	NP_005912.1:p.Ser232=
XM_005248519.3:c.318T>A	XP_005248576.2:p.Ser106=
XM_011543406.1:c.441T>A	XP_011541708.1:p.Ser147=
XM_011543407.1:c.696T>A	XP_011541709.1:p.Ser232=
XM_011543408.1:c.696T>A	XP_011541710.1:p.Ser232=
XM_017009484.1:c.285T>A	XP_016864973.1:p.Ser95=
XM_017009485.1:c.207T>A	XP_016864974.1:p.Ser69=
XR_001742068.2:n.727T>A
NM_005921.2:c.696T>A MANE Select	NP_005912.1:p.Ser232=