Canonical Allele Identifier: CA359787582

Gene: MAP3K1

Linked Data

• dbSNP Id: rs746611474
• MyVariant Identifiers: chr5:g.56178094C>A (hg19) ; chr5:g.56882267C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882267C>A , CM000667.2:g.56882267C>A	GRCh38
NC_000005.9:g.56178094C>A , CM000667.1:g.56178094C>A	GRCh37
NC_000005.8:g.56213851C>A	NCBI36
NG_031884.1:g.72195C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3067C>A MANE Select	ENSP00000382423.3:p.Arg1023Ser
ENST00000399503.3:c.3067C>A	ENSP00000382423.3:p.Arg1023Ser
NM_005921.1:c.3067C>A	NP_005912.1:p.Arg1023Ser
XM_005248519.3:c.2689C>A	XP_005248576.2:p.Arg897Ser
XM_011543406.1:c.2812C>A	XP_011541708.1:p.Arg938Ser
XM_011543407.1:c.2788C>A	XP_011541709.1:p.Arg930Ser
XM_011543408.1:c.3067C>A	XP_011541710.1:p.Arg1023Ser
XM_017009484.1:c.2656C>A	XP_016864973.1:p.Arg886Ser
XM_017009485.1:c.2578C>A	XP_016864974.1:p.Arg860Ser
XR_001742068.2:n.3098C>A
NM_005921.2:c.3067C>A MANE Select	NP_005912.1:p.Arg1023Ser