Canonical Allele Identifier: CA2635986331

Gene: CTC1

Linked Data

• gnomAD v4: 17-8237292-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8237298_8237300del , CM000679.2:g.8237298_8237300del	GRCh38
NC_000017.10:g.8140616_8140618del , CM000679.1:g.8140616_8140618del	GRCh37
NC_000017.9:g.8081341_8081343del	NCBI36
NG_032148.1:g.15801_15803del
NG_032148.2:g.15801_15803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.792+80_792+82del	ENSP00000462607.2:n.792+80_792+82del
ENST00000581729.2:c.792+80_792+82del	ENSP00000462720.2:n.792+80_792+82del
ENST00000581967.2:n.814+80_814+82del
ENST00000583254.2:n.206+80_206+82del
ENST00000699849.1:c.-106+80_-106+82del	ENSP00000514647.1:n.-106+80_-106+82del
ENST00000699850.1:n.56-953_56-951del
ENST00000699851.1:n.814+80_814+82del
ENST00000699852.1:c.792+80_792+82del	ENSP00000514648.1:n.792+80_792+82del
ENST00000699853.1:c.792+80_792+82del	ENSP00000514649.1:n.792+80_792+82del
ENST00000699854.1:n.585+80_585+82del
ENST00000699855.1:n.814+80_814+82del
ENST00000699856.1:c.792+80_792+82del	ENSP00000514650.1:n.792+80_792+82del
ENST00000699857.1:n.800+80_800+82del
ENST00000699858.1:c.792+80_792+82del	ENSP00000514651.1:n.792+80_792+82del
ENST00000699859.1:c.792+80_792+82del	ENSP00000514652.1:n.792+80_792+82del
ENST00000699861.1:n.814+80_814+82del
ENST00000699862.1:n.679+80_679+82del
ENST00000449476.7:c.687+80_687+82del	ENSP00000396018.2:n.687+80_687+82del
ENST00000581671.2:n.633+80_633+82del
ENST00000643543.1:c.792+80_792+82del	ENSP00000494323.1:n.792+80_792+82del
ENST00000651323.1:c.792+80_792+82del MANE Select	ENSP00000498499.1:n.792+80_792+82del
ENST00000315684.12:c.792+80_792+82del	ENSP00000313759.8:n.792+80_792+82del
ENST00000449476.6:c.687+80_687+82del	ENSP00000396018.2:n.687+80_687+82del
ENST00000581671.1:n.633+80_633+82del
NM_025099.5:c.792+80_792+82del	NP_079375.3:n.792+80_792+82del
NR_046431.1:n.746+80_746+82del
XM_006721577.2:c.792+80_792+82del	XP_006721640.1:n.792+80_792+82del
XM_006721578.2:c.792+80_792+82del	XP_006721641.1:n.792+80_792+82del
XM_006721579.2:c.792+80_792+82del	XP_006721642.1:n.792+80_792+82del
XM_011524010.1:c.687+80_687+82del	XP_011522312.1:n.687+80_687+82del
XM_011524011.1:c.-110+80_-110+82del	XP_011522313.1:n.-110+80_-110+82del
XR_429823.2:n.835+80_835+82del
XR_429824.2:n.835+80_835+82del
XR_429825.1:n.835+80_835+82del
NM_025099.6:c.792+80_792+82del MANE Select	NP_079375.3:n.792+80_792+82del
XM_006721577.3:c.792+80_792+82del	XP_006721640.1:n.792+80_792+82del
XM_006721578.3:c.792+80_792+82del	XP_006721641.1:n.792+80_792+82del
XM_011524010.2:c.687+80_687+82del	XP_011522312.1:n.687+80_687+82del
XM_011524011.2:c.-110+80_-110+82del	XP_011522313.1:n.-110+80_-110+82del
XR_001752639.1:n.835+80_835+82del
XR_001752640.1:n.835+80_835+82del
XR_001752641.1:n.835+80_835+82del
XR_001752642.1:n.835+80_835+82del
XR_001752643.1:n.835+80_835+82del
XR_001752644.1:n.835+80_835+82del
XR_002958073.1:n.835+80_835+82del
XR_429823.3:n.835+80_835+82del
XR_429824.3:n.835+80_835+82del
NR_046431.2:n.707+80_707+82del