Canonical Allele Identifier: CA359787618

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178112T>C (hg19) ; chr5:g.56882285T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882285T>C , CM000667.2:g.56882285T>C	GRCh38
NC_000005.9:g.56178112T>C , CM000667.1:g.56178112T>C	GRCh37
NC_000005.8:g.56213869T>C	NCBI36
NG_031884.1:g.72213T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3085T>C MANE Select	ENSP00000382423.3:p.Phe1029Leu
ENST00000399503.3:c.3085T>C	ENSP00000382423.3:p.Phe1029Leu
NM_005921.1:c.3085T>C	NP_005912.1:p.Phe1029Leu
XM_005248519.3:c.2707T>C	XP_005248576.2:p.Phe903Leu
XM_011543406.1:c.2830T>C	XP_011541708.1:p.Phe944Leu
XM_011543407.1:c.2806T>C	XP_011541709.1:p.Phe936Leu
XM_011543408.1:c.3085T>C	XP_011541710.1:p.Phe1029Leu
XM_017009484.1:c.2674T>C	XP_016864973.1:p.Phe892Leu
XM_017009485.1:c.2596T>C	XP_016864974.1:p.Phe866Leu
XR_001742068.2:n.3116T>C
NM_005921.2:c.3085T>C MANE Select	NP_005912.1:p.Phe1029Leu