Canonical Allele Identifier: CA359802598

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155683G>A (hg19) ; chr5:g.56859856G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859856G>A , CM000667.2:g.56859856G>A	GRCh38
NC_000005.9:g.56155683G>A , CM000667.1:g.56155683G>A	GRCh37
NC_000005.8:g.56191440G>A	NCBI36
NG_031884.1:g.49784G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.775G>A MANE Select	ENSP00000382423.3:p.Gly259Ser
ENST00000399503.3:c.775G>A	ENSP00000382423.3:p.Gly259Ser
NM_005921.1:c.775G>A	NP_005912.1:p.Gly259Ser
XM_005248519.3:c.397G>A	XP_005248576.2:p.Gly133Ser
XM_011543406.1:c.520G>A	XP_011541708.1:p.Gly174Ser
XM_011543407.1:c.775G>A	XP_011541709.1:p.Gly259Ser
XM_011543408.1:c.775G>A	XP_011541710.1:p.Gly259Ser
XM_017009484.1:c.364G>A	XP_016864973.1:p.Gly122Ser
XM_017009485.1:c.286G>A	XP_016864974.1:p.Gly96Ser
XR_001742068.2:n.806G>A
NM_005921.2:c.775G>A MANE Select	NP_005912.1:p.Gly259Ser