Canonical Allele Identifier: CA10650519

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8227622C>T , CM000679.2:g.8227622C>T	GRCh38
NC_000017.10:g.8130940C>T , CM000679.1:g.8130940C>T	GRCh37
NC_000017.9:g.8071665C>T	NCBI36
NG_032148.1:g.25474G>A
NG_032148.2:g.25474G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*558G>A MANE Select	NP_079375.3:n.*558G>A
ENST00000651323.1:c.*558G>A MANE Select	ENSP00000498499.1:n.*558G>A
NM_025099.5:c.*558G>A	NP_079375.3:n.*558G>A
NR_046431.1:n.4101G>A
NR_046431.2:n.4062G>A
ENST00000315684.12:c.*558G>A	ENSP00000313759.8:n.*558G>A
ENST00000449476.6:c.*946G>A	ENSP00000396018.2:n.*946G>A
ENST00000449476.7:c.*946G>A	ENSP00000396018.2:n.*946G>A
ENST00000643543.1:c.*2919G>A	ENSP00000494323.1:n.*2919G>A
ENST00000699849.1:c.*558G>A	ENSP00000514647.1:n.*558G>A
ENST00000699850.1:n.4144G>A
ENST00000699851.1:n.5098G>A
ENST00000699852.1:c.*2725G>A	ENSP00000514648.1:n.*2725G>A
ENST00000699853.1:c.*797G>A	ENSP00000514649.1:n.*797G>A
XM_006721577.2:c.*558G>A	XP_006721640.1:n.*558G>A
XM_006721577.3:c.*558G>A	XP_006721640.1:n.*558G>A
XM_006721578.2:c.*558G>A	XP_006721641.1:n.*558G>A
XM_006721578.3:c.*558G>A	XP_006721641.1:n.*558G>A
XM_011524010.1:c.*558G>A	XP_011522312.1:n.*558G>A
XM_011524010.2:c.*558G>A	XP_011522312.1:n.*558G>A
XM_011524011.1:c.*558G>A	XP_011522313.1:n.*558G>A
XM_011524011.2:c.*558G>A	XP_011522313.1:n.*558G>A
XR_001752639.1:n.4063G>A
XR_001752640.1:n.4211G>A
XR_001752641.1:n.4146G>A
XR_001752642.1:n.3996G>A
XR_002958073.1:n.4502G>A
XR_429823.2:n.4089G>A
XR_429823.3:n.4089G>A
XR_429824.2:n.4190G>A
XR_429824.3:n.4190G>A