Canonical Allele Identifier: CA444399118

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177526G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881699G>C , CM000667.2:g.56881699G>C	GRCh38
NC_000005.9:g.56177526G>C , CM000667.1:g.56177526G>C	GRCh37
NC_000005.8:g.56213283G>C	NCBI36
NG_031884.1:g.71627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2499G>C MANE Select	ENSP00000382423.3:p.Val833=
ENST00000399503.3:c.2499G>C	ENSP00000382423.3:p.Val833=
NM_005921.1:c.2499G>C	NP_005912.1:p.Val833=
XM_005248519.3:c.2121G>C	XP_005248576.2:p.Val707=
XM_011543406.1:c.2244G>C	XP_011541708.1:p.Val748=
XM_011543407.1:c.2220G>C	XP_011541709.1:p.Val740=
XM_011543408.1:c.2499G>C	XP_011541710.1:p.Val833=
XM_017009484.1:c.2088G>C	XP_016864973.1:p.Val696=
XM_017009485.1:c.2010G>C	XP_016864974.1:p.Val670=
XR_001742068.2:n.2530G>C
NM_005921.2:c.2499G>C MANE Select	NP_005912.1:p.Val833=