Canonical Allele Identifier: CA1174413861

Gene: CTH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70439157C= , CM000663.2:g.70439157C=	GRCh38
NC_000001.10:g.70904840C= , CM000663.1:g.70904840C=	GRCh37
NC_000001.9:g.70677428C=	NCBI36
NG_008041.1:g.32886C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370938.8:c.*30C= MANE Select	ENSP00000359976.3:n.*30C=
ENST00000346806.2:c.*30C=	ENSP00000311554.2:n.*30C=
ENST00000370938.7:c.*30C=	ENSP00000359976.3:n.*30C=
ENST00000411986.6:c.*30C=	ENSP00000413407.2:n.*30C=
ENST00000482383.1:n.523C=
NM_001190463.1:c.*30C=	NP_001177392.1:n.*30C=
NM_001902.5:c.*30C=	NP_001893.2:n.*30C=
NM_153742.4:c.*30C=	NP_714964.2:n.*30C=
XM_005270509.2:c.*30C=	XP_005270566.1:n.*30C=
XM_011540787.1:c.*30C=	XP_011539089.1:n.*30C=
XM_005270509.3:c.*30C=	XP_005270566.1:n.*30C=
XM_017000416.2:c.*30C=	XP_016855905.1:n.*30C=
NM_001902.6:c.*30C= MANE Select	NP_001893.2:n.*30C=
NM_001190463.2:c.*30C=	NP_001177392.1:n.*30C=
NM_153742.5:c.*30C=	NP_714964.2:n.*30C=