Canonical Allele Identifier: CA444398922

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171122G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875295G>C , CM000667.2:g.56875295G>C	GRCh38
NC_000005.9:g.56171122G>C , CM000667.1:g.56171122G>C	GRCh37
NC_000005.8:g.56206879G>C	NCBI36
NG_031884.1:g.65223G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1950G>C MANE Select	ENSP00000382423.3:p.Val650=
ENST00000399503.3:c.1950G>C	ENSP00000382423.3:p.Val650=
NM_005921.1:c.1950G>C	NP_005912.1:p.Val650=
XM_005248519.3:c.1572G>C	XP_005248576.2:p.Val524=
XM_011543406.1:c.1695G>C	XP_011541708.1:p.Val565=
XM_011543407.1:c.1686+2290G>C	XP_011541709.1:n.1686+2290G>C
XM_011543408.1:c.1950G>C	XP_011541710.1:p.Val650=
XM_017009484.1:c.1539G>C	XP_016864973.1:p.Val513=
XM_017009485.1:c.1461G>C	XP_016864974.1:p.Val487=
XR_001742068.2:n.1981G>C
NM_005921.2:c.1950G>C MANE Select	NP_005912.1:p.Val650=