Canonical Allele Identifier: CA2635986460

Gene: CTC1

Linked Data

• gnomAD v4: 17-8237359-T-TTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8237359_8237360insTAA , CM000679.2:g.8237359_8237360insTAA	GRCh38
NC_000017.10:g.8140677_8140678insTAA , CM000679.1:g.8140677_8140678insTAA	GRCh37
NC_000017.9:g.8081402_8081403insTAA	NCBI36
NG_032148.1:g.15736_15737insTTA
NG_032148.2:g.15736_15737insTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.792+15_792+16insTTA	ENSP00000462607.2:n.792+15_792+16insTTA
ENST00000581729.2:c.792+15_792+16insTTA	ENSP00000462720.2:n.792+15_792+16insTTA
ENST00000581967.2:n.814+15_814+16insTTA
ENST00000583254.2:n.206+15_206+16insTTA
ENST00000699849.1:c.-106+15_-106+16insTTA	ENSP00000514647.1:n.-106+15_-106+16insTTA
ENST00000699850.1:n.56-1018_56-1017insTTA
ENST00000699851.1:n.814+15_814+16insTTA
ENST00000699852.1:c.792+15_792+16insTTA	ENSP00000514648.1:n.792+15_792+16insTTA
ENST00000699853.1:c.792+15_792+16insTTA	ENSP00000514649.1:n.792+15_792+16insTTA
ENST00000699854.1:n.585+15_585+16insTTA
ENST00000699855.1:n.814+15_814+16insTTA
ENST00000699856.1:c.792+15_792+16insTTA	ENSP00000514650.1:n.792+15_792+16insTTA
ENST00000699857.1:n.800+15_800+16insTTA
ENST00000699858.1:c.792+15_792+16insTTA	ENSP00000514651.1:n.792+15_792+16insTTA
ENST00000699859.1:c.792+15_792+16insTTA	ENSP00000514652.1:n.792+15_792+16insTTA
ENST00000699861.1:n.814+15_814+16insTTA
ENST00000699862.1:n.679+15_679+16insTTA
ENST00000449476.7:c.687+15_687+16insTTA	ENSP00000396018.2:n.687+15_687+16insTTA
ENST00000581671.2:n.633+15_633+16insTTA
ENST00000643543.1:c.792+15_792+16insTTA	ENSP00000494323.1:n.792+15_792+16insTTA
ENST00000651323.1:c.792+15_792+16insTTA MANE Select	ENSP00000498499.1:n.792+15_792+16insTTA
ENST00000315684.12:c.792+15_792+16insTTA	ENSP00000313759.8:n.792+15_792+16insTTA
ENST00000449476.6:c.687+15_687+16insTTA	ENSP00000396018.2:n.687+15_687+16insTTA
ENST00000581671.1:n.633+15_633+16insTTA
NM_025099.5:c.792+15_792+16insTTA	NP_079375.3:n.792+15_792+16insTTA
NR_046431.1:n.746+15_746+16insTTA
XM_006721577.2:c.792+15_792+16insTTA	XP_006721640.1:n.792+15_792+16insTTA
XM_006721578.2:c.792+15_792+16insTTA	XP_006721641.1:n.792+15_792+16insTTA
XM_006721579.2:c.792+15_792+16insTTA	XP_006721642.1:n.792+15_792+16insTTA
XM_011524010.1:c.687+15_687+16insTTA	XP_011522312.1:n.687+15_687+16insTTA
XM_011524011.1:c.-110+15_-110+16insTTA	XP_011522313.1:n.-110+15_-110+16insTTA
XR_429823.2:n.835+15_835+16insTTA
XR_429824.2:n.835+15_835+16insTTA
XR_429825.1:n.835+15_835+16insTTA
NM_025099.6:c.792+15_792+16insTTA MANE Select	NP_079375.3:n.792+15_792+16insTTA
XM_006721577.3:c.792+15_792+16insTTA	XP_006721640.1:n.792+15_792+16insTTA
XM_006721578.3:c.792+15_792+16insTTA	XP_006721641.1:n.792+15_792+16insTTA
XM_011524010.2:c.687+15_687+16insTTA	XP_011522312.1:n.687+15_687+16insTTA
XM_011524011.2:c.-110+15_-110+16insTTA	XP_011522313.1:n.-110+15_-110+16insTTA
XR_001752639.1:n.835+15_835+16insTTA
XR_001752640.1:n.835+15_835+16insTTA
XR_001752641.1:n.835+15_835+16insTTA
XR_001752642.1:n.835+15_835+16insTTA
XR_001752643.1:n.835+15_835+16insTTA
XR_001752644.1:n.835+15_835+16insTTA
XR_002958073.1:n.835+15_835+16insTTA
XR_429823.3:n.835+15_835+16insTTA
XR_429824.3:n.835+15_835+16insTTA
NR_046431.2:n.707+15_707+16insTTA