Canonical Allele Identifier: CA444399696

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178118A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882291A>C , CM000667.2:g.56882291A>C	GRCh38
NC_000005.9:g.56178118A>C , CM000667.1:g.56178118A>C	GRCh37
NC_000005.8:g.56213875A>C	NCBI36
NG_031884.1:g.72219A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3091A>C MANE Select	ENSP00000382423.3:p.Arg1031=
ENST00000399503.3:c.3091A>C	ENSP00000382423.3:p.Arg1031=
NM_005921.1:c.3091A>C	NP_005912.1:p.Arg1031=
XM_005248519.3:c.2713A>C	XP_005248576.2:p.Arg905=
XM_011543406.1:c.2836A>C	XP_011541708.1:p.Arg946=
XM_011543407.1:c.2812A>C	XP_011541709.1:p.Arg938=
XM_011543408.1:c.3091A>C	XP_011541710.1:p.Arg1031=
XM_017009484.1:c.2680A>C	XP_016864973.1:p.Arg894=
XM_017009485.1:c.2602A>C	XP_016864974.1:p.Arg868=
XR_001742068.2:n.3122A>C
NM_005921.2:c.3091A>C MANE Select	NP_005912.1:p.Arg1031=