Canonical Allele Identifier: CA444398797

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171041C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875214C>A , CM000667.2:g.56875214C>A	GRCh38
NC_000005.9:g.56171041C>A , CM000667.1:g.56171041C>A	GRCh37
NC_000005.8:g.56206798C>A	NCBI36
NG_031884.1:g.65142C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1869C>A MANE Select	ENSP00000382423.3:p.Ser623=
ENST00000399503.3:c.1869C>A	ENSP00000382423.3:p.Ser623=
NM_005921.1:c.1869C>A	NP_005912.1:p.Ser623=
XM_005248519.3:c.1491C>A	XP_005248576.2:p.Ser497=
XM_011543406.1:c.1614C>A	XP_011541708.1:p.Ser538=
XM_011543407.1:c.1686+2209C>A	XP_011541709.1:n.1686+2209C>A
XM_011543408.1:c.1869C>A	XP_011541710.1:p.Ser623=
XM_017009484.1:c.1458C>A	XP_016864973.1:p.Ser486=
XM_017009485.1:c.1380C>A	XP_016864974.1:p.Ser460=
XR_001742068.2:n.1900C>A
NM_005921.2:c.1869C>A MANE Select	NP_005912.1:p.Ser623=