Canonical Allele Identifier: CA359781055

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1172032327
• gnomAD v3: 5-56875204-G-C
• gnomAD v4: 5-56875204-G-C
• MyVariant Identifiers: chr5:g.56171031G>C (hg19) ; chr5:g.56875204G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875204G>C , CM000667.2:g.56875204G>C	GRCh38
NC_000005.9:g.56171031G>C , CM000667.1:g.56171031G>C	GRCh37
NC_000005.8:g.56206788G>C	NCBI36
NG_031884.1:g.65132G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1859G>C MANE Select	ENSP00000382423.3:p.Ser620Thr
ENST00000399503.3:c.1859G>C	ENSP00000382423.3:p.Ser620Thr
NM_005921.1:c.1859G>C	NP_005912.1:p.Ser620Thr
XM_005248519.3:c.1481G>C	XP_005248576.2:p.Ser494Thr
XM_011543406.1:c.1604G>C	XP_011541708.1:p.Ser535Thr
XM_011543407.1:c.1686+2199G>C	XP_011541709.1:n.1686+2199G>C
XM_011543408.1:c.1859G>C	XP_011541710.1:p.Ser620Thr
XM_017009484.1:c.1448G>C	XP_016864973.1:p.Ser483Thr
XM_017009485.1:c.1370G>C	XP_016864974.1:p.Ser457Thr
XR_001742068.2:n.1890G>C
NM_005921.2:c.1859G>C MANE Select	NP_005912.1:p.Ser620Thr