Canonical Allele Identifier: CA1174413867

Gene: CTH

Linked Data

• dbSNP Id: rs1684666513
• gnomAD v4: 1-70439169-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70439169A>T , CM000663.2:g.70439169A>T	GRCh38
NC_000001.10:g.70904852A>T , CM000663.1:g.70904852A>T	GRCh37
NC_000001.9:g.70677440A>T	NCBI36
NG_008041.1:g.32898A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370938.8:c.*42A>T MANE Select	ENSP00000359976.3:n.*42A>T
ENST00000346806.2:c.*42A>T	ENSP00000311554.2:n.*42A>T
ENST00000370938.7:c.*42A>T	ENSP00000359976.3:n.*42A>T
ENST00000411986.6:c.*42A>T	ENSP00000413407.2:n.*42A>T
ENST00000482383.1:n.535A>T
NM_001190463.1:c.*42A>T	NP_001177392.1:n.*42A>T
NM_001902.5:c.*42A>T	NP_001893.2:n.*42A>T
NM_153742.4:c.*42A>T	NP_714964.2:n.*42A>T
XM_005270509.2:c.*42A>T	XP_005270566.1:n.*42A>T
XM_011540787.1:c.*42A>T	XP_011539089.1:n.*42A>T
XM_005270509.3:c.*42A>T	XP_005270566.1:n.*42A>T
XM_017000416.2:c.*42A>T	XP_016855905.1:n.*42A>T
NM_001902.6:c.*42A>T MANE Select	NP_001893.2:n.*42A>T
NM_001190463.2:c.*42A>T	NP_001177392.1:n.*42A>T
NM_153742.5:c.*42A>T	NP_714964.2:n.*42A>T