Canonical Allele Identifier: CA359785753

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177445T>A (hg19) ; chr5:g.56881618T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881618T>A , CM000667.2:g.56881618T>A	GRCh38
NC_000005.9:g.56177445T>A , CM000667.1:g.56177445T>A	GRCh37
NC_000005.8:g.56213202T>A	NCBI36
NG_031884.1:g.71546T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2418T>A MANE Select	ENSP00000382423.3:p.Asp806Glu
ENST00000399503.3:c.2418T>A	ENSP00000382423.3:p.Asp806Glu
NM_005921.1:c.2418T>A	NP_005912.1:p.Asp806Glu
XM_005248519.3:c.2040T>A	XP_005248576.2:p.Asp680Glu
XM_011543406.1:c.2163T>A	XP_011541708.1:p.Asp721Glu
XM_011543407.1:c.2139T>A	XP_011541709.1:p.Asp713Glu
XM_011543408.1:c.2418T>A	XP_011541710.1:p.Asp806Glu
XM_017009484.1:c.2007T>A	XP_016864973.1:p.Asp669Glu
XM_017009485.1:c.1929T>A	XP_016864974.1:p.Asp643Glu
XR_001742068.2:n.2449T>A
NM_005921.2:c.2418T>A MANE Select	NP_005912.1:p.Asp806Glu