Canonical Allele Identifier: CA287525875

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8225101G>A , CM000679.2:g.8225101G>A	GRCh38
NC_000017.10:g.8128419G>A , CM000679.1:g.8128419G>A	GRCh37
NC_000017.9:g.8069144G>A	NCBI36
NG_032148.1:g.27995C>T
NG_032148.2:g.27995C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*3079C>T MANE Select	NP_079375.3:n.*3079C>T
ENST00000651323.1:c.*3079C>T MANE Select	ENSP00000498499.1:n.*3079C>T
NM_025099.5:c.*3079C>T	NP_079375.3:n.*3079C>T
NR_046431.1:n.6622C>T
NR_046431.2:n.6583C>T
ENST00000315684.12:c.*3079C>T	ENSP00000313759.8:n.*3079C>T
XM_006721577.3:c.*3079C>T	XP_006721640.1:n.*3079C>T
XM_006721578.3:c.*3079C>T	XP_006721641.1:n.*3079C>T
XM_011524010.2:c.*3079C>T	XP_011522312.1:n.*3079C>T
XM_011524011.2:c.*3079C>T	XP_011522313.1:n.*3079C>T
XR_001752639.1:n.6584C>T
XR_001752640.1:n.6732C>T
XR_001752641.1:n.6667C>T
XR_001752642.1:n.6517C>T
XR_002958073.1:n.7023C>T
XR_429823.3:n.6610C>T
XR_429824.3:n.6711C>T