Canonical Allele Identifier: CA1174413823

Gene: CTH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70439057C= , CM000663.2:g.70439057C=	GRCh38
NC_000001.10:g.70904740C= , CM000663.1:g.70904740C=	GRCh37
NC_000001.9:g.70677328C=	NCBI36
NG_008041.1:g.32786C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370938.8:c.1192-44C= MANE Select	ENSP00000359976.3:n.1192-44C=
ENST00000346806.2:c.1060-44C=	ENSP00000311554.2:n.1060-44C=
ENST00000370938.7:c.1192-44C=	ENSP00000359976.3:n.1192-44C=
ENST00000411986.6:c.1096-44C=	ENSP00000413407.2:n.1096-44C=
ENST00000482383.1:n.467-44C=
NM_001190463.1:c.1096-44C=	NP_001177392.1:n.1096-44C=
NM_001902.5:c.1192-44C=	NP_001893.2:n.1192-44C=
NM_153742.4:c.1060-44C=	NP_714964.2:n.1060-44C=
XM_005270509.2:c.865-44C=	XP_005270566.1:n.865-44C=
XM_011540787.1:c.622-44C=	XP_011539089.1:n.622-44C=
XM_005270509.3:c.865-44C=	XP_005270566.1:n.865-44C=
XM_017000416.2:c.622-44C=	XP_016855905.1:n.622-44C=
NM_001902.6:c.1192-44C= MANE Select	NP_001893.2:n.1192-44C=
NM_001190463.2:c.1096-44C=	NP_001177392.1:n.1096-44C=
NM_153742.5:c.1060-44C=	NP_714964.2:n.1060-44C=