Canonical Allele Identifier: CA8372646

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8238460C>A , CM000679.2:g.8238460C>A	GRCh38
NC_000017.10:g.8141778C>A , CM000679.1:g.8141778C>A	GRCh37
NC_000017.9:g.8082503C>A	NCBI36
NG_032148.1:g.14636G>T
NG_032148.2:g.14636G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.367G>T MANE Select	NP_079375.3:p.Asp123Tyr
ENST00000651323.1:c.367G>T MANE Select	ENSP00000498499.1:p.Asp123Tyr
NM_025099.5:c.367G>T	NP_079375.3:p.Asp123Tyr
NR_046431.1:n.426G>T
NR_046431.2:n.387G>T
ENST00000315684.12:c.367G>T	ENSP00000313759.8:p.Asp123Tyr
ENST00000449476.6:c.367G>T	ENSP00000396018.2:p.Asp123Tyr
ENST00000449476.7:c.367G>T	ENSP00000396018.2:p.Asp123Tyr
ENST00000580299.2:c.367G>T	ENSP00000462607.2:p.Asp123Tyr
ENST00000581671.1:n.208G>T
ENST00000581671.2:n.208G>T
ENST00000581729.2:c.367G>T	ENSP00000462720.2:p.Asp123Tyr
ENST00000581967.2:n.389G>T
ENST00000584842.1:n.310G>T
ENST00000643543.1:c.367G>T	ENSP00000494323.1:p.Asp123Tyr
ENST00000699849.1:c.-531G>T	ENSP00000514647.1:n.-531G>T
ENST00000699850.1:n.56-2118G>T
ENST00000699851.1:n.389G>T
ENST00000699852.1:c.367G>T	ENSP00000514648.1:p.Asp123Tyr
ENST00000699853.1:c.367G>T	ENSP00000514649.1:p.Asp123Tyr
ENST00000699854.1:n.160G>T
ENST00000699855.1:n.389G>T
ENST00000699856.1:c.367G>T	ENSP00000514650.1:p.Asp123Tyr
ENST00000699857.1:n.375G>T
ENST00000699858.1:c.367G>T	ENSP00000514651.1:p.Asp123Tyr
ENST00000699859.1:c.367G>T	ENSP00000514652.1:p.Asp123Tyr
ENST00000699861.1:n.389G>T
ENST00000699862.1:n.254G>T
XM_006721577.2:c.367G>T	XP_006721640.1:p.Asp123Tyr
XM_006721577.3:c.367G>T	XP_006721640.1:p.Asp123Tyr
XM_006721578.2:c.367G>T	XP_006721641.1:p.Asp123Tyr
XM_006721578.3:c.367G>T	XP_006721641.1:p.Asp123Tyr
XM_006721579.2:c.367G>T	XP_006721642.1:p.Asp123Tyr
XM_011524010.1:c.367G>T	XP_011522312.1:p.Asp123Tyr
XM_011524010.2:c.367G>T	XP_011522312.1:p.Asp123Tyr
XM_011524011.1:c.-323G>T	XP_011522313.1:n.-323G>T
XM_011524011.2:c.-323G>T	XP_011522313.1:n.-323G>T
XR_001752639.1:n.410G>T
XR_001752640.1:n.410G>T
XR_001752641.1:n.410G>T
XR_001752642.1:n.410G>T
XR_001752643.1:n.410G>T
XR_001752644.1:n.410G>T
XR_002958073.1:n.410G>T
XR_429823.2:n.410G>T
XR_429823.3:n.410G>T
XR_429824.2:n.410G>T
XR_429824.3:n.410G>T
XR_429825.1:n.410G>T