Canonical Allele Identifier: CA444399191

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177694T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881867T>A , CM000667.2:g.56881867T>A	GRCh38
NC_000005.9:g.56177694T>A , CM000667.1:g.56177694T>A	GRCh37
NC_000005.8:g.56213451T>A	NCBI36
NG_031884.1:g.71795T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2667T>A MANE Select	ENSP00000382423.3:p.Val889=
ENST00000399503.3:c.2667T>A	ENSP00000382423.3:p.Val889=
NM_005921.1:c.2667T>A	NP_005912.1:p.Val889=
XM_005248519.3:c.2289T>A	XP_005248576.2:p.Val763=
XM_011543406.1:c.2412T>A	XP_011541708.1:p.Val804=
XM_011543407.1:c.2388T>A	XP_011541709.1:p.Val796=
XM_011543408.1:c.2667T>A	XP_011541710.1:p.Val889=
XM_017009484.1:c.2256T>A	XP_016864973.1:p.Val752=
XM_017009485.1:c.2178T>A	XP_016864974.1:p.Val726=
XR_001742068.2:n.2698T>A
NM_005921.2:c.2667T>A MANE Select	NP_005912.1:p.Val889=