Canonical Allele Identifier: CA340839868

Gene: CTH

Linked Data

• MyVariant Identifiers: chr1:g.70904803A>G (hg19) ; chr1:g.70439120A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70439120A>G , CM000663.2:g.70439120A>G	GRCh38
NC_000001.10:g.70904803A>G , CM000663.1:g.70904803A>G	GRCh37
NC_000001.9:g.70677391A>G	NCBI36
NG_008041.1:g.32849A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370938.8:c.1211A>G MANE Select	ENSP00000359976.3:p.His404Arg
ENST00000346806.2:c.1079A>G	ENSP00000311554.2:p.His360Arg
ENST00000370938.7:c.1211A>G	ENSP00000359976.3:p.His404Arg
ENST00000411986.6:c.1115A>G	ENSP00000413407.2:p.His372Arg
ENST00000482383.1:n.486A>G
NM_001190463.1:c.1115A>G	NP_001177392.1:p.His372Arg
NM_001902.5:c.1211A>G	NP_001893.2:p.His404Arg
NM_153742.4:c.1079A>G	NP_714964.2:p.His360Arg
XM_005270509.2:c.884A>G	XP_005270566.1:p.His295Arg
XM_011540787.1:c.641A>G	XP_011539089.1:p.His214Arg
XM_005270509.3:c.884A>G	XP_005270566.1:p.His295Arg
XM_017000416.2:c.641A>G	XP_016855905.1:p.His214Arg
NM_001902.6:c.1211A>G MANE Select	NP_001893.2:p.His404Arg
NM_001190463.2:c.1115A>G	NP_001177392.1:p.His372Arg
NM_153742.5:c.1079A>G	NP_714964.2:p.His360Arg