Canonical Allele Identifier: CA656472288

Gene: CTC1

Linked Data

• COSMIC: COSN4892916

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231708A>G , CM000679.2:g.8231708A>G	GRCh38
NC_000017.10:g.8135026A>G , CM000679.1:g.8135026A>G	GRCh37
NC_000017.9:g.8075751A>G	NCBI36
NG_032148.1:g.21388T>C
NG_032148.2:g.21388T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2475+18T>C	ENSP00000462607.2:n.2475+18T>C
ENST00000581729.2:c.2475+18T>C	ENSP00000462720.2:n.2475+18T>C
ENST00000581967.2:n.2927+18T>C
ENST00000583254.2:n.3286T>C
ENST00000699849.1:c.1578+18T>C	ENSP00000514647.1:n.1578+18T>C
ENST00000699850.1:n.1738+18T>C
ENST00000699851.1:n.2497+18T>C
ENST00000699852.1:c.*1151+18T>C	ENSP00000514648.1:n.*1151+18T>C
ENST00000699853.1:c.2475+18T>C	ENSP00000514649.1:n.2475+18T>C
ENST00000699854.1:n.2268+18T>C
ENST00000699855.1:n.2927+18T>C
ENST00000699856.1:c.2475+18T>C	ENSP00000514650.1:n.2475+18T>C
ENST00000699857.1:n.2483+18T>C
ENST00000699858.1:c.*1088+18T>C	ENSP00000514651.1:n.*1088+18T>C
ENST00000699859.1:c.2346+18T>C	ENSP00000514652.1:n.2346+18T>C
ENST00000699860.1:n.581+18T>C
ENST00000699861.1:n.2497+18T>C
ENST00000699862.1:n.3435+18T>C
ENST00000449476.7:c.2370+18T>C	ENSP00000396018.2:n.2370+18T>C
ENST00000581671.2:n.2464+18T>C
ENST00000643543.1:c.*1182+18T>C	ENSP00000494323.1:n.*1182+18T>C
ENST00000651323.1:c.2475+18T>C MANE Select	ENSP00000498499.1:n.2475+18T>C
ENST00000315684.12:c.2475+18T>C	ENSP00000313759.8:n.2475+18T>C
ENST00000449476.6:c.2370+18T>C	ENSP00000396018.2:n.2370+18T>C
ENST00000578240.1:n.703+18T>C
ENST00000578537.1:c.371+18T>C
NM_025099.5:c.2475+18T>C	NP_079375.3:n.2475+18T>C
NR_046431.1:n.2429+18T>C
XM_006721577.2:c.2346+18T>C	XP_006721640.1:n.2346+18T>C
XM_006721578.2:c.2475+18T>C	XP_006721641.1:n.2475+18T>C
XM_006721579.2:c.2475+18T>C	XP_006721642.1:n.2475+18T>C
XM_011524010.1:c.2370+18T>C	XP_011522312.1:n.2370+18T>C
XM_011524011.1:c.1578+18T>C	XP_011522313.1:n.1578+18T>C
XR_429823.2:n.2518+18T>C
XR_429824.2:n.2518+18T>C
XR_429825.1:n.2518+18T>C
NM_025099.6:c.2475+18T>C MANE Select	NP_079375.3:n.2475+18T>C
XM_006721577.3:c.2346+18T>C	XP_006721640.1:n.2346+18T>C
XM_006721578.3:c.2475+18T>C	XP_006721641.1:n.2475+18T>C
XM_011524010.2:c.2370+18T>C	XP_011522312.1:n.2370+18T>C
XM_011524011.2:c.1578+18T>C	XP_011522313.1:n.1578+18T>C
XR_001752639.1:n.2389+18T>C
XR_001752640.1:n.2518+18T>C
XR_001752641.1:n.2518+18T>C
XR_001752642.1:n.2518+18T>C
XR_001752643.1:n.2948+18T>C
XR_002958073.1:n.2518+18T>C
XR_429823.3:n.2518+18T>C
XR_429824.3:n.2518+18T>C
NR_046431.2:n.2390+18T>C