Canonical Allele Identifier: CA287527857

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8226811T>C , CM000679.2:g.8226811T>C	GRCh38
NC_000017.10:g.8130129T>C , CM000679.1:g.8130129T>C	GRCh37
NC_000017.9:g.8070854T>C	NCBI36
NG_032148.1:g.26285A>G
NG_032148.2:g.26285A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*1369A>G MANE Select	NP_079375.3:n.*1369A>G
ENST00000651323.1:c.*1369A>G MANE Select	ENSP00000498499.1:n.*1369A>G
NM_025099.5:c.*1369A>G	NP_079375.3:n.*1369A>G
NR_046431.1:n.4912A>G
NR_046431.2:n.4873A>G
ENST00000315684.12:c.*1369A>G	ENSP00000313759.8:n.*1369A>G
XM_006721577.2:c.*1369A>G	XP_006721640.1:n.*1369A>G
XM_006721577.3:c.*1369A>G	XP_006721640.1:n.*1369A>G
XM_006721578.2:c.*1369A>G	XP_006721641.1:n.*1369A>G
XM_006721578.3:c.*1369A>G	XP_006721641.1:n.*1369A>G
XM_011524010.1:c.*1369A>G	XP_011522312.1:n.*1369A>G
XM_011524010.2:c.*1369A>G	XP_011522312.1:n.*1369A>G
XM_011524011.1:c.*1369A>G	XP_011522313.1:n.*1369A>G
XM_011524011.2:c.*1369A>G	XP_011522313.1:n.*1369A>G
XR_001752639.1:n.4874A>G
XR_001752640.1:n.5022A>G
XR_001752641.1:n.4957A>G
XR_001752642.1:n.4807A>G
XR_002958073.1:n.5313A>G
XR_429823.2:n.4900A>G
XR_429823.3:n.4900A>G
XR_429824.2:n.5001A>G
XR_429824.3:n.5001A>G