Canonical Allele Identifier: CA2635985312

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231681-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231681_8231682insT , CM000679.2:g.8231681_8231682insT	GRCh38
NC_000017.10:g.8134999_8135000insT , CM000679.1:g.8134999_8135000insT	GRCh37
NC_000017.9:g.8075724_8075725insT	NCBI36
NG_032148.1:g.21414_21415insA
NG_032148.2:g.21414_21415insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2475+44_2475+45insA	ENSP00000462607.2:n.2475+44_2475+45insA
ENST00000581729.2:c.2475+44_2475+45insA	ENSP00000462720.2:n.2475+44_2475+45insA
ENST00000581967.2:n.2927+44_2927+45insA
ENST00000583254.2:n.3312_3313insA
ENST00000699849.1:c.1578+44_1578+45insA	ENSP00000514647.1:n.1578+44_1578+45insA
ENST00000699850.1:n.1738+44_1738+45insA
ENST00000699851.1:n.2497+44_2497+45insA
ENST00000699852.1:c.*1151+44_*1151+45insA	ENSP00000514648.1:n.*1151+44_*1151+45insA
ENST00000699853.1:c.2475+44_2475+45insA	ENSP00000514649.1:n.2475+44_2475+45insA
ENST00000699854.1:n.2268+44_2268+45insA
ENST00000699855.1:n.2927+44_2927+45insA
ENST00000699856.1:c.2475+44_2475+45insA	ENSP00000514650.1:n.2475+44_2475+45insA
ENST00000699857.1:n.2483+44_2483+45insA
ENST00000699858.1:c.*1088+44_*1088+45insA	ENSP00000514651.1:n.*1088+44_*1088+45insA
ENST00000699859.1:c.2346+44_2346+45insA	ENSP00000514652.1:n.2346+44_2346+45insA
ENST00000699860.1:n.581+44_581+45insA
ENST00000699861.1:n.2497+44_2497+45insA
ENST00000699862.1:n.3435+44_3435+45insA
ENST00000449476.7:c.2370+44_2370+45insA	ENSP00000396018.2:n.2370+44_2370+45insA
ENST00000581671.2:n.2464+44_2464+45insA
ENST00000643543.1:c.*1182+44_*1182+45insA	ENSP00000494323.1:n.*1182+44_*1182+45insA
ENST00000651323.1:c.2475+44_2475+45insA MANE Select	ENSP00000498499.1:n.2475+44_2475+45insA
ENST00000315684.12:c.2475+44_2475+45insA	ENSP00000313759.8:n.2475+44_2475+45insA
ENST00000449476.6:c.2370+44_2370+45insA	ENSP00000396018.2:n.2370+44_2370+45insA
ENST00000578240.1:n.703+44_703+45insA
ENST00000578537.1:c.371+44_371+45insA
NM_025099.5:c.2475+44_2475+45insA	NP_079375.3:n.2475+44_2475+45insA
NR_046431.1:n.2429+44_2429+45insA
XM_006721577.2:c.2346+44_2346+45insA	XP_006721640.1:n.2346+44_2346+45insA
XM_006721578.2:c.2475+44_2475+45insA	XP_006721641.1:n.2475+44_2475+45insA
XM_006721579.2:c.2475+44_2475+45insA	XP_006721642.1:n.2475+44_2475+45insA
XM_011524010.1:c.2370+44_2370+45insA	XP_011522312.1:n.2370+44_2370+45insA
XM_011524011.1:c.1578+44_1578+45insA	XP_011522313.1:n.1578+44_1578+45insA
XR_429823.2:n.2518+44_2518+45insA
XR_429824.2:n.2518+44_2518+45insA
XR_429825.1:n.2518+44_2518+45insA
NM_025099.6:c.2475+44_2475+45insA MANE Select	NP_079375.3:n.2475+44_2475+45insA
XM_006721577.3:c.2346+44_2346+45insA	XP_006721640.1:n.2346+44_2346+45insA
XM_006721578.3:c.2475+44_2475+45insA	XP_006721641.1:n.2475+44_2475+45insA
XM_011524010.2:c.2370+44_2370+45insA	XP_011522312.1:n.2370+44_2370+45insA
XM_011524011.2:c.1578+44_1578+45insA	XP_011522313.1:n.1578+44_1578+45insA
XR_001752639.1:n.2389+44_2389+45insA
XR_001752640.1:n.2518+44_2518+45insA
XR_001752641.1:n.2518+44_2518+45insA
XR_001752642.1:n.2518+44_2518+45insA
XR_001752643.1:n.2948+44_2948+45insA
XR_002958073.1:n.2518+44_2518+45insA
XR_429823.3:n.2518+44_2518+45insA
XR_429824.3:n.2518+44_2518+45insA
NR_046431.2:n.2390+44_2390+45insA