Canonical Allele Identifier: CA10651349

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8226706C>T , CM000679.2:g.8226706C>T	GRCh38
NC_000017.10:g.8130024C>T , CM000679.1:g.8130024C>T	GRCh37
NC_000017.9:g.8070749C>T	NCBI36
NG_032148.1:g.26390G>A
NG_032148.2:g.26390G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651323.1:c.*1474G>A MANE Select	ENSP00000498499.1:n.*1474G>A
ENST00000315684.12:c.*1474G>A	ENSP00000313759.8:n.*1474G>A
NM_025099.5:c.*1474G>A	NP_079375.3:n.*1474G>A
NR_046431.1:n.5017G>A
XM_006721577.2:c.*1474G>A	XP_006721640.1:n.*1474G>A
XM_006721578.2:c.*1474G>A	XP_006721641.1:n.*1474G>A
XM_011524010.1:c.*1474G>A	XP_011522312.1:n.*1474G>A
XM_011524011.1:c.*1474G>A	XP_011522313.1:n.*1474G>A
XR_429823.2:n.5005G>A
XR_429824.2:n.5106G>A
NM_025099.6:c.*1474G>A MANE Select	NP_079375.3:n.*1474G>A
XM_006721577.3:c.*1474G>A	XP_006721640.1:n.*1474G>A
XM_006721578.3:c.*1474G>A	XP_006721641.1:n.*1474G>A
XM_011524010.2:c.*1474G>A	XP_011522312.1:n.*1474G>A
XM_011524011.2:c.*1474G>A	XP_011522313.1:n.*1474G>A
XR_001752639.1:n.4979G>A
XR_001752640.1:n.5127G>A
XR_001752641.1:n.5062G>A
XR_001752642.1:n.4912G>A
XR_002958073.1:n.5418G>A
XR_429823.3:n.5005G>A
XR_429824.3:n.5106G>A
NR_046431.2:n.4978G>A