Canonical Allele Identifier: CA1140495644

Gene: CTH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70430388C= , CM000663.2:g.70430388C=	GRCh38
NC_000001.10:g.70896071C= , CM000663.1:g.70896071C=	GRCh37
NC_000001.9:g.70668659C=	NCBI36
NG_008041.1:g.24117C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370938.8:c.718C= MANE Select	ENSP00000359976.3:p.Gln240=
ENST00000346806.2:c.586C=	ENSP00000311554.2:p.Gln196=
ENST00000370938.7:c.718C=	ENSP00000359976.3:p.Gln240=
ENST00000411986.6:c.622C=	ENSP00000413407.2:p.Gln208=
ENST00000464926.1:n.766C=
NM_001190463.1:c.622C=	NP_001177392.1:p.Gln208=
NM_001902.5:c.718C=	NP_001893.2:p.Gln240=
NM_153742.4:c.586C=	NP_714964.2:p.Gln196=
XM_005270509.2:c.391C=	XP_005270566.1:p.Gln131=
XM_011540787.1:c.148C=	XP_011539089.1:p.Gln50=
XM_005270509.3:c.391C=	XP_005270566.1:p.Gln131=
XM_017000416.2:c.148C=	XP_016855905.1:p.Gln50=
NM_001902.6:c.718C= MANE Select	NP_001893.2:p.Gln240=
NM_001190463.2:c.622C=	NP_001177392.1:p.Gln208=
NM_153742.5:c.586C=	NP_714964.2:p.Gln196=