Canonical Allele Identifier: CA287528861

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8227706C>T , CM000679.2:g.8227706C>T	GRCh38
NC_000017.10:g.8131024C>T , CM000679.1:g.8131024C>T	GRCh37
NC_000017.9:g.8071749C>T	NCBI36
NG_032148.1:g.25390G>A
NG_032148.2:g.25390G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*474G>A MANE Select	NP_079375.3:n.*474G>A
ENST00000651323.1:c.*474G>A MANE Select	ENSP00000498499.1:n.*474G>A
NM_025099.5:c.*474G>A	NP_079375.3:n.*474G>A
NR_046431.1:n.4017G>A
NR_046431.2:n.3978G>A
ENST00000315684.12:c.*474G>A	ENSP00000313759.8:n.*474G>A
ENST00000449476.6:c.*862G>A	ENSP00000396018.2:n.*862G>A
ENST00000449476.7:c.*862G>A	ENSP00000396018.2:n.*862G>A
ENST00000643543.1:c.*2835G>A	ENSP00000494323.1:n.*2835G>A
ENST00000699849.1:c.*474G>A	ENSP00000514647.1:n.*474G>A
ENST00000699850.1:n.4060G>A
ENST00000699851.1:n.5014G>A
ENST00000699852.1:c.*2641G>A	ENSP00000514648.1:n.*2641G>A
ENST00000699853.1:c.*713G>A	ENSP00000514649.1:n.*713G>A
XM_006721577.2:c.*474G>A	XP_006721640.1:n.*474G>A
XM_006721577.3:c.*474G>A	XP_006721640.1:n.*474G>A
XM_006721578.2:c.*474G>A	XP_006721641.1:n.*474G>A
XM_006721578.3:c.*474G>A	XP_006721641.1:n.*474G>A
XM_011524010.1:c.*474G>A	XP_011522312.1:n.*474G>A
XM_011524010.2:c.*474G>A	XP_011522312.1:n.*474G>A
XM_011524011.1:c.*474G>A	XP_011522313.1:n.*474G>A
XM_011524011.2:c.*474G>A	XP_011522313.1:n.*474G>A
XR_001752639.1:n.3979G>A
XR_001752640.1:n.4127G>A
XR_001752641.1:n.4062G>A
XR_001752642.1:n.3912G>A
XR_002958073.1:n.4418G>A
XR_429823.2:n.4005G>A
XR_429823.3:n.4005G>A
XR_429824.2:n.4106G>A
XR_429824.3:n.4106G>A