Canonical Allele Identifier: CA444399783

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178144A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882317A>C , CM000667.2:g.56882317A>C	GRCh38
NC_000005.9:g.56178144A>C , CM000667.1:g.56178144A>C	GRCh37
NC_000005.8:g.56213901A>C	NCBI36
NG_031884.1:g.72245A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3117A>C MANE Select	ENSP00000382423.3:p.Ser1039=
ENST00000399503.3:c.3117A>C	ENSP00000382423.3:p.Ser1039=
NM_005921.1:c.3117A>C	NP_005912.1:p.Ser1039=
XM_005248519.3:c.2739A>C	XP_005248576.2:p.Ser913=
XM_011543406.1:c.2862A>C	XP_011541708.1:p.Ser954=
XM_011543407.1:c.2838A>C	XP_011541709.1:p.Ser946=
XM_011543408.1:c.3117A>C	XP_011541710.1:p.Ser1039=
XM_017009484.1:c.2706A>C	XP_016864973.1:p.Ser902=
XM_017009485.1:c.2628A>C	XP_016864974.1:p.Ser876=
XR_001742068.2:n.3148A>C
NM_005921.2:c.3117A>C MANE Select	NP_005912.1:p.Ser1039=