Canonical Allele Identifier: CA287527022

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8226469T>C , CM000679.2:g.8226469T>C	GRCh38
NC_000017.10:g.8129787T>C , CM000679.1:g.8129787T>C	GRCh37
NC_000017.9:g.8070512T>C	NCBI36
NG_032148.1:g.26627A>G
NG_032148.2:g.26627A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*1711A>G MANE Select	NP_079375.3:n.*1711A>G
ENST00000651323.1:c.*1711A>G MANE Select	ENSP00000498499.1:n.*1711A>G
NM_025099.5:c.*1711A>G	NP_079375.3:n.*1711A>G
NR_046431.1:n.5254A>G
NR_046431.2:n.5215A>G
ENST00000315684.12:c.*1711A>G	ENSP00000313759.8:n.*1711A>G
XM_006721577.2:c.*1711A>G	XP_006721640.1:n.*1711A>G
XM_006721577.3:c.*1711A>G	XP_006721640.1:n.*1711A>G
XM_006721578.2:c.*1711A>G	XP_006721641.1:n.*1711A>G
XM_006721578.3:c.*1711A>G	XP_006721641.1:n.*1711A>G
XM_011524010.1:c.*1711A>G	XP_011522312.1:n.*1711A>G
XM_011524010.2:c.*1711A>G	XP_011522312.1:n.*1711A>G
XM_011524011.1:c.*1711A>G	XP_011522313.1:n.*1711A>G
XM_011524011.2:c.*1711A>G	XP_011522313.1:n.*1711A>G
XR_001752639.1:n.5216A>G
XR_001752640.1:n.5364A>G
XR_001752641.1:n.5299A>G
XR_001752642.1:n.5149A>G
XR_002958073.1:n.5655A>G
XR_429823.2:n.5242A>G
XR_429823.3:n.5242A>G
XR_429824.2:n.5343A>G
XR_429824.3:n.5343A>G