Canonical Allele Identifier: CA359787878

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56882402-G-A
• MyVariant Identifiers: chr5:g.56178229G>A (hg19) ; chr5:g.56882402G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882402G>A , CM000667.2:g.56882402G>A	GRCh38
NC_000005.9:g.56178229G>A , CM000667.1:g.56178229G>A	GRCh37
NC_000005.8:g.56213986G>A	NCBI36
NG_031884.1:g.72330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3202G>A MANE Select	ENSP00000382423.3:p.Gly1068Ser
ENST00000399503.3:c.3202G>A	ENSP00000382423.3:p.Gly1068Ser
NM_005921.1:c.3202G>A	NP_005912.1:p.Gly1068Ser
XM_005248519.3:c.2824G>A	XP_005248576.2:p.Gly942Ser
XM_011543406.1:c.2947G>A	XP_011541708.1:p.Gly983Ser
XM_011543407.1:c.2923G>A	XP_011541709.1:p.Gly975Ser
XM_011543408.1:c.3202G>A	XP_011541710.1:p.Gly1068Ser
XM_017009484.1:c.2791G>A	XP_016864973.1:p.Gly931Ser
XM_017009485.1:c.2713G>A	XP_016864974.1:p.Gly905Ser
XR_001742068.2:n.3233G>A
NM_005921.2:c.3202G>A MANE Select	NP_005912.1:p.Gly1068Ser