Canonical Allele Identifier: CA1364890088

Gene: STAB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52506696G= , CM000665.2:g.52506696G=	GRCh38
NC_000003.11:g.52540712G= , CM000665.1:g.52540712G=	GRCh37
NC_000003.10:g.52515752G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321725.10:c.1835G= MANE Select	ENSP00000312946.6:p.Arg612=
ENST00000481607.1:n.1890G=
NM_015136.2:c.1835G=	NP_055951.2:p.Arg612=
XM_005264973.2:c.1835G=	XP_005265030.1:p.Arg612=
XM_005264974.2:c.1835G=	XP_005265031.1:p.Arg612=
XM_005264975.2:c.1835G=	XP_005265032.1:p.Arg612=
XM_006713065.1:c.1835G=	XP_006713128.1:p.Arg612=
XM_011533528.1:c.1835G=	XP_011531830.1:p.Arg612=
XR_940395.1:n.1911G=
XM_005264973.3:c.1835G=	XP_005265030.1:p.Arg612=
XM_017005998.1:c.1835G=	XP_016861487.1:p.Arg612=
XM_017005999.1:c.1835G=	XP_016861488.1:p.Arg612=
XM_017006000.1:c.1835G=	XP_016861489.1:p.Arg612=
XM_017006001.1:c.1835G=	XP_016861490.1:p.Arg612=
XM_017006002.1:c.1835G=	XP_016861491.1:p.Arg612=
XM_017006003.1:c.1835G=	XP_016861492.1:p.Arg612=
XM_017006004.2:c.1835G=	XP_016861493.1:p.Arg612=
XR_001740064.1:n.1911G=
NM_015136.3:c.1835G= MANE Select	NP_055951.2:p.Arg612=