Canonical Allele Identifier: CA444399504

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748248643
• MyVariant Identifiers: chr5:g.56178204G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882377G>A , CM000667.2:g.56882377G>A	GRCh38
NC_000005.9:g.56178204G>A , CM000667.1:g.56178204G>A	GRCh37
NC_000005.8:g.56213961G>A	NCBI36
NG_031884.1:g.72305G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3177G>A MANE Select	ENSP00000382423.3:p.Arg1059=
ENST00000399503.3:c.3177G>A	ENSP00000382423.3:p.Arg1059=
NM_005921.1:c.3177G>A	NP_005912.1:p.Arg1059=
XM_005248519.3:c.2799G>A	XP_005248576.2:p.Arg933=
XM_011543406.1:c.2922G>A	XP_011541708.1:p.Arg974=
XM_011543407.1:c.2898G>A	XP_011541709.1:p.Arg966=
XM_011543408.1:c.3177G>A	XP_011541710.1:p.Arg1059=
XM_017009484.1:c.2766G>A	XP_016864973.1:p.Arg922=
XM_017009485.1:c.2688G>A	XP_016864974.1:p.Arg896=
XR_001742068.2:n.3208G>A
NM_005921.2:c.3177G>A MANE Select	NP_005912.1:p.Arg1059=