Canonical Allele Identifier: CA359787690

Gene: MAP3K1

Linked Data

• dbSNP Id: rs148803468
• MyVariant Identifiers: chr5:g.56178142T>A (hg19) ; chr5:g.56882315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882315T>A , CM000667.2:g.56882315T>A	GRCh38
NC_000005.9:g.56178142T>A , CM000667.1:g.56178142T>A	GRCh37
NC_000005.8:g.56213899T>A	NCBI36
NG_031884.1:g.72243T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3115T>A MANE Select	ENSP00000382423.3:p.Ser1039Thr
ENST00000399503.3:c.3115T>A	ENSP00000382423.3:p.Ser1039Thr
NM_005921.1:c.3115T>A	NP_005912.1:p.Ser1039Thr
XM_005248519.3:c.2737T>A	XP_005248576.2:p.Ser913Thr
XM_011543406.1:c.2860T>A	XP_011541708.1:p.Ser954Thr
XM_011543407.1:c.2836T>A	XP_011541709.1:p.Ser946Thr
XM_011543408.1:c.3115T>A	XP_011541710.1:p.Ser1039Thr
XM_017009484.1:c.2704T>A	XP_016864973.1:p.Ser902Thr
XM_017009485.1:c.2626T>A	XP_016864974.1:p.Ser876Thr
XR_001742068.2:n.3146T>A
NM_005921.2:c.3115T>A MANE Select	NP_005912.1:p.Ser1039Thr