Canonical Allele Identifier: CA2635985048

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231497-TGTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231501_8231504del , CM000679.2:g.8231501_8231504del	GRCh38
NC_000017.10:g.8134819_8134822del , CM000679.1:g.8134819_8134822del	GRCh37
NC_000017.9:g.8075544_8075547del	NCBI36
NG_032148.1:g.21595_21598del
NG_032148.2:g.21595_21598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2476-32_2476-29del	ENSP00000462607.2:n.2476-32_2476-29del
ENST00000581729.2:c.2476-32_2476-29del	ENSP00000462720.2:n.2476-32_2476-29del
ENST00000581967.2:n.2928-32_2928-29del
ENST00000583254.2:n.3493_3496del
ENST00000699849.1:c.1579-32_1579-29del	ENSP00000514647.1:n.1579-32_1579-29del
ENST00000699850.1:n.1739-32_1739-29del
ENST00000699851.1:n.2498-32_2498-29del
ENST00000699852.1:c.*1152-32_*1152-29del	ENSP00000514648.1:n.*1152-32_*1152-29del
ENST00000699853.1:c.2476-32_2476-29del	ENSP00000514649.1:n.2476-32_2476-29del
ENST00000699854.1:n.2269-32_2269-29del
ENST00000699855.1:n.2928-32_2928-29del
ENST00000699856.1:c.2476-32_2476-29del	ENSP00000514650.1:n.2476-32_2476-29del
ENST00000699857.1:n.2484-32_2484-29del
ENST00000699858.1:c.*1089-32_*1089-29del	ENSP00000514651.1:n.*1089-32_*1089-29del
ENST00000699859.1:c.2347-32_2347-29del	ENSP00000514652.1:n.2347-32_2347-29del
ENST00000699860.1:n.581+225_581+228del
ENST00000699861.1:n.2498-32_2498-29del
ENST00000699862.1:n.3436-32_3436-29del
ENST00000449476.7:c.2371-32_2371-29del	ENSP00000396018.2:n.2371-32_2371-29del
ENST00000581671.2:n.2465-32_2465-29del
ENST00000643543.1:c.*1183-32_*1183-29del	ENSP00000494323.1:n.*1183-32_*1183-29del
ENST00000651323.1:c.2476-32_2476-29del MANE Select	ENSP00000498499.1:n.2476-32_2476-29del
ENST00000315684.12:c.2476-32_2476-29del	ENSP00000313759.8:n.2476-32_2476-29del
ENST00000449476.6:c.2371-32_2371-29del	ENSP00000396018.2:n.2371-32_2371-29del
ENST00000578240.1:n.704-32_704-29del
ENST00000578537.1:c.371+225_371+228del
NM_025099.5:c.2476-32_2476-29del	NP_079375.3:n.2476-32_2476-29del
NR_046431.1:n.2430-32_2430-29del
XM_006721577.2:c.2347-32_2347-29del	XP_006721640.1:n.2347-32_2347-29del
XM_006721578.2:c.2476-32_2476-29del	XP_006721641.1:n.2476-32_2476-29del
XM_006721579.2:c.2476-32_2476-29del	XP_006721642.1:n.2476-32_2476-29del
XM_011524010.1:c.2371-32_2371-29del	XP_011522312.1:n.2371-32_2371-29del
XM_011524011.1:c.1579-32_1579-29del	XP_011522313.1:n.1579-32_1579-29del
XR_429823.2:n.2519-32_2519-29del
XR_429824.2:n.2519-32_2519-29del
XR_429825.1:n.2518+225_2518+228del
NM_025099.6:c.2476-32_2476-29del MANE Select	NP_079375.3:n.2476-32_2476-29del
XM_006721577.3:c.2347-32_2347-29del	XP_006721640.1:n.2347-32_2347-29del
XM_006721578.3:c.2476-32_2476-29del	XP_006721641.1:n.2476-32_2476-29del
XM_011524010.2:c.2371-32_2371-29del	XP_011522312.1:n.2371-32_2371-29del
XM_011524011.2:c.1579-32_1579-29del	XP_011522313.1:n.1579-32_1579-29del
XR_001752639.1:n.2390-32_2390-29del
XR_001752640.1:n.2519-32_2519-29del
XR_001752641.1:n.2519-32_2519-29del
XR_001752642.1:n.2518+225_2518+228del
XR_001752643.1:n.2949-32_2949-29del
XR_002958073.1:n.2518+225_2518+228del
XR_429823.3:n.2519-32_2519-29del
XR_429824.3:n.2519-32_2519-29del
NR_046431.2:n.2391-32_2391-29del