Canonical Allele Identifier: CA397967629

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228236A>T , CM000679.2:g.8228236A>T	GRCh38
NC_000017.10:g.8131554A>T , CM000679.1:g.8131554A>T	GRCh37
NC_000017.9:g.8072279A>T	NCBI36
NG_032148.1:g.24860T>A
NG_032148.2:g.24860T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.3334T>A	ENSP00000462607.2:p.Ser1112Thr
ENST00000581729.2:c.3367T>A	ENSP00000462720.2:p.Ser1123Thr
ENST00000699849.1:c.2470T>A	ENSP00000514647.1:p.Ser824Thr
ENST00000699850.1:n.3530T>A
ENST00000699851.1:n.4484T>A
ENST00000699852.1:c.*2111T>A	ENSP00000514648.1:n.*2111T>A
ENST00000699853.1:c.*183T>A	ENSP00000514649.1:n.*183T>A
ENST00000699854.1:n.4157T>A
ENST00000699855.1:n.4721T>A
ENST00000699856.1:c.*549T>A	ENSP00000514650.1:n.*549T>A
ENST00000699857.1:n.4177T>A
ENST00000699858.1:c.*2882T>A	ENSP00000514651.1:n.*2882T>A
ENST00000699859.1:c.*334T>A	ENSP00000514652.1:n.*334T>A
ENST00000699860.1:n.2276T>A
ENST00000699861.1:n.4061T>A
ENST00000449476.7:c.*332T>A	ENSP00000396018.2:n.*332T>A
ENST00000581671.2:n.3587T>A
ENST00000643543.1:c.*2305T>A	ENSP00000494323.1:n.*2305T>A
ENST00000651323.1:c.3598T>A MANE Select	ENSP00000498499.1:p.Ser1200Thr
ENST00000315684.12:c.3598T>A	ENSP00000313759.8:p.Ser1200Thr
ENST00000449476.6:c.*332T>A	ENSP00000396018.2:n.*332T>A
ENST00000581729.1:c.315T>A
NM_025099.5:c.3598T>A	NP_079375.3:p.Ser1200Thr
NR_046431.1:n.3487T>A
XM_006721577.2:c.3469T>A	XP_006721640.1:p.Ser1157Thr
XM_006721578.2:c.3367T>A	XP_006721641.1:p.Ser1123Thr
XM_011524010.1:c.3493T>A	XP_011522312.1:p.Ser1165Thr
XM_011524011.1:c.2701T>A	XP_011522313.1:p.Ser901Thr
XR_429823.2:n.3475T>A
XR_429824.2:n.3576T>A
NM_025099.6:c.3598T>A MANE Select	NP_079375.3:p.Ser1200Thr
XM_006721577.3:c.3469T>A	XP_006721640.1:p.Ser1157Thr
XM_006721578.3:c.3367T>A	XP_006721641.1:p.Ser1123Thr
XM_011524010.2:c.3493T>A	XP_011522312.1:p.Ser1165Thr
XM_011524011.2:c.2701T>A	XP_011522313.1:p.Ser901Thr
XR_001752639.1:n.3449T>A
XR_001752640.1:n.3597T>A
XR_001752641.1:n.3532T>A
XR_001752642.1:n.3382T>A
XR_002958073.1:n.3888T>A
XR_429823.3:n.3475T>A
XR_429824.3:n.3576T>A
NR_046431.2:n.3448T>A