Canonical Allele Identifier: CA1174411183

Gene: CTH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70432151C= , CM000663.2:g.70432151C=	GRCh38
NC_000001.10:g.70897834C= , CM000663.1:g.70897834C=	GRCh37
NC_000001.9:g.70670422C=	NCBI36
NG_008041.1:g.25880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370938.8:c.793C= MANE Select	ENSP00000359976.3:p.Arg265=
ENST00000346806.2:c.661C=	ENSP00000311554.2:p.Arg221=
ENST00000370938.7:c.793C=	ENSP00000359976.3:p.Arg265=
ENST00000411986.6:c.697C=	ENSP00000413407.2:p.Arg233=
NM_001190463.1:c.697C=	NP_001177392.1:p.Arg233=
NM_001902.5:c.793C=	NP_001893.2:p.Arg265=
NM_153742.4:c.661C=	NP_714964.2:p.Arg221=
XM_005270509.2:c.466C=	XP_005270566.1:p.Arg156=
XM_011540787.1:c.223C=	XP_011539089.1:p.Arg75=
XM_005270509.3:c.466C=	XP_005270566.1:p.Arg156=
XM_017000416.2:c.223C=	XP_016855905.1:p.Arg75=
NM_001902.6:c.793C= MANE Select	NP_001893.2:p.Arg265=
NM_001190463.2:c.697C=	NP_001177392.1:p.Arg233=
NM_153742.5:c.661C=	NP_714964.2:p.Arg221=