Canonical Allele Identifier: CA444399122

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177532A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881705A>T , CM000667.2:g.56881705A>T	GRCh38
NC_000005.9:g.56177532A>T , CM000667.1:g.56177532A>T	GRCh37
NC_000005.8:g.56213289A>T	NCBI36
NG_031884.1:g.71633A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2505A>T MANE Select	ENSP00000382423.3:p.Ser835=
ENST00000399503.3:c.2505A>T	ENSP00000382423.3:p.Ser835=
NM_005921.1:c.2505A>T	NP_005912.1:p.Ser835=
XM_005248519.3:c.2127A>T	XP_005248576.2:p.Ser709=
XM_011543406.1:c.2250A>T	XP_011541708.1:p.Ser750=
XM_011543407.1:c.2226A>T	XP_011541709.1:p.Ser742=
XM_011543408.1:c.2505A>T	XP_011541710.1:p.Ser835=
XM_017009484.1:c.2094A>T	XP_016864973.1:p.Ser698=
XM_017009485.1:c.2016A>T	XP_016864974.1:p.Ser672=
XR_001742068.2:n.2536A>T
NM_005921.2:c.2505A>T MANE Select	NP_005912.1:p.Ser835=