Canonical Allele Identifier: CA359787620

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178113T>A (hg19) ; chr5:g.56882286T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882286T>A , CM000667.2:g.56882286T>A	GRCh38
NC_000005.9:g.56178113T>A , CM000667.1:g.56178113T>A	GRCh37
NC_000005.8:g.56213870T>A	NCBI36
NG_031884.1:g.72214T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3086T>A MANE Select	ENSP00000382423.3:p.Phe1029Tyr
ENST00000399503.3:c.3086T>A	ENSP00000382423.3:p.Phe1029Tyr
NM_005921.1:c.3086T>A	NP_005912.1:p.Phe1029Tyr
XM_005248519.3:c.2708T>A	XP_005248576.2:p.Phe903Tyr
XM_011543406.1:c.2831T>A	XP_011541708.1:p.Phe944Tyr
XM_011543407.1:c.2807T>A	XP_011541709.1:p.Phe936Tyr
XM_011543408.1:c.3086T>A	XP_011541710.1:p.Phe1029Tyr
XM_017009484.1:c.2675T>A	XP_016864973.1:p.Phe892Tyr
XM_017009485.1:c.2597T>A	XP_016864974.1:p.Phe866Tyr
XR_001742068.2:n.3117T>A
NM_005921.2:c.3086T>A MANE Select	NP_005912.1:p.Phe1029Tyr