Canonical Allele Identifier: CA2246189172

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231463T= , CM000679.2:g.8231463T=	GRCh38
NC_000017.10:g.8134781T= , CM000679.1:g.8134781T=	GRCh37
NC_000017.9:g.8075506T=	NCBI36
NG_032148.1:g.21633A=
NG_032148.2:g.21633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2482A=	ENSP00000462607.2:p.Met828=
ENST00000581729.2:c.2482A=	ENSP00000462720.2:p.Met828=
ENST00000581967.2:n.2934A=
ENST00000583254.2:n.3531A=
ENST00000699849.1:c.1585A=	ENSP00000514647.1:p.Met529=
ENST00000699850.1:n.1745A=
ENST00000699851.1:n.2504A=
ENST00000699852.1:c.*1158A=	ENSP00000514648.1:n.*1158A=
ENST00000699853.1:c.2482A=	ENSP00000514649.1:p.Met828=
ENST00000699854.1:n.2275A=
ENST00000699855.1:n.2934A=
ENST00000699856.1:c.2482A=	ENSP00000514650.1:p.Met828=
ENST00000699857.1:n.2490A=
ENST00000699858.1:c.*1095A=	ENSP00000514651.1:n.*1095A=
ENST00000699859.1:c.2353A=	ENSP00000514652.1:p.Met785=
ENST00000699860.1:n.581+263A=
ENST00000699861.1:n.2504A=
ENST00000699862.1:n.3442A=
ENST00000449476.7:c.2377A=	ENSP00000396018.2:p.Met793=
ENST00000581671.2:n.2471A=
ENST00000643543.1:c.*1189A=	ENSP00000494323.1:n.*1189A=
ENST00000651323.1:c.2482A= MANE Select	ENSP00000498499.1:p.Met828=
ENST00000315684.12:c.2482A=	ENSP00000313759.8:p.Met828=
ENST00000449476.6:c.2377A=	ENSP00000396018.2:p.Met793=
ENST00000578240.1:n.710A=
ENST00000578537.1:c.371+263A=
NM_025099.5:c.2482A=	NP_079375.3:p.Met828=
NR_046431.1:n.2436A=
XM_006721577.2:c.2353A=	XP_006721640.1:p.Met785=
XM_006721578.2:c.2482A=	XP_006721641.1:p.Met828=
XM_006721579.2:c.2482A=	XP_006721642.1:p.Met828=
XM_011524010.1:c.2377A=	XP_011522312.1:p.Met793=
XM_011524011.1:c.1585A=	XP_011522313.1:p.Met529=
XR_429823.2:n.2525A=
XR_429824.2:n.2525A=
XR_429825.1:n.2518+263A=
NM_025099.6:c.2482A= MANE Select	NP_079375.3:p.Met828=
XM_006721577.3:c.2353A=	XP_006721640.1:p.Met785=
XM_006721578.3:c.2482A=	XP_006721641.1:p.Met828=
XM_011524010.2:c.2377A=	XP_011522312.1:p.Met793=
XM_011524011.2:c.1585A=	XP_011522313.1:p.Met529=
XR_001752639.1:n.2396A=
XR_001752640.1:n.2525A=
XR_001752641.1:n.2525A=
XR_001752642.1:n.2518+263A=
XR_001752643.1:n.2955A=
XR_002958073.1:n.2518+263A=
XR_429823.3:n.2525A=
XR_429824.3:n.2525A=
NR_046431.2:n.2397A=