Canonical Allele Identifier: CA1140495643

Gene: CTH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70415987C= , CM000663.2:g.70415987C=	GRCh38
NC_000001.10:g.70881670C= , CM000663.1:g.70881670C=	GRCh37
NC_000001.9:g.70654258C=	NCBI36
NG_008041.1:g.9716C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001902.6:c.200C= MANE Select	NP_001893.2:p.Thr67=
ENST00000370938.8:c.200C= MANE Select	ENSP00000359976.3:p.Thr67=
NM_001190463.1:c.200C=	NP_001177392.1:p.Thr67=
NM_001190463.2:c.200C=	NP_001177392.1:p.Thr67=
NM_001902.5:c.200C=	NP_001893.2:p.Thr67=
NM_153742.4:c.200C=	NP_714964.2:p.Thr67=
NM_153742.5:c.200C=	NP_714964.2:p.Thr67=
ENST00000346806.2:c.200C=	ENSP00000311554.2:p.Thr67=
ENST00000370938.7:c.200C=	ENSP00000359976.3:p.Thr67=
ENST00000411986.6:c.200C=	ENSP00000413407.2:p.Thr67=
ENST00000464926.1:n.344C=
XM_005270509.2:c.-128C=	XP_005270566.1:n.-128C=
XM_005270509.3:c.-128C=	XP_005270566.1:n.-128C=