Canonical Allele Identifier: CA1548136431

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875191G= , CM000667.2:g.56875191G=	GRCh38
NC_000005.9:g.56171018G= , CM000667.1:g.56171018G=	GRCh37
NC_000005.8:g.56206775G=	NCBI36
NG_031884.1:g.65119G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1846G= MANE Select	ENSP00000382423.3:p.Gly616=
ENST00000399503.3:c.1846G=	ENSP00000382423.3:p.Gly616=
NM_005921.1:c.1846G=	NP_005912.1:p.Gly616=
XM_005248519.3:c.1468G=	XP_005248576.2:p.Gly490=
XM_011543406.1:c.1591G=	XP_011541708.1:p.Gly531=
XM_011543407.1:c.1686+2186G=	XP_011541709.1:n.1686+2186G=
XM_011543408.1:c.1846G=	XP_011541710.1:p.Gly616=
XM_017009484.1:c.1435G=	XP_016864973.1:p.Gly479=
XM_017009485.1:c.1357G=	XP_016864974.1:p.Gly453=
XR_001742068.2:n.1877G=
NM_005921.2:c.1846G= MANE Select	NP_005912.1:p.Gly616=