Canonical Allele Identifier: CA359787792

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178190A>C (hg19) ; chr5:g.56882363A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882363A>C , CM000667.2:g.56882363A>C	GRCh38
NC_000005.9:g.56178190A>C , CM000667.1:g.56178190A>C	GRCh37
NC_000005.8:g.56213947A>C	NCBI36
NG_031884.1:g.72291A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3163A>C MANE Select	ENSP00000382423.3:p.Ser1055Arg
ENST00000399503.3:c.3163A>C	ENSP00000382423.3:p.Ser1055Arg
NM_005921.1:c.3163A>C	NP_005912.1:p.Ser1055Arg
XM_005248519.3:c.2785A>C	XP_005248576.2:p.Ser929Arg
XM_011543406.1:c.2908A>C	XP_011541708.1:p.Ser970Arg
XM_011543407.1:c.2884A>C	XP_011541709.1:p.Ser962Arg
XM_011543408.1:c.3163A>C	XP_011541710.1:p.Ser1055Arg
XM_017009484.1:c.2752A>C	XP_016864973.1:p.Ser918Arg
XM_017009485.1:c.2674A>C	XP_016864974.1:p.Ser892Arg
XR_001742068.2:n.3194A>C
NM_005921.2:c.3163A>C MANE Select	NP_005912.1:p.Ser1055Arg