Canonical Allele Identifier: CA497958691

Gene: CTC1

Linked Data

• dbSNP Id: rs1439552225
• gnomAD v2: 17-8134608-G-A
• gnomAD v4: 17-8231290-G-A
• MyVariant Identifiers: chr17:g.8134608G>A (hg19) ; chr17:g.8231290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231290G>A , CM000679.2:g.8231290G>A	GRCh38
NC_000017.10:g.8134608G>A , CM000679.1:g.8134608G>A	GRCh37
NC_000017.9:g.8075333G>A	NCBI36
NG_032148.1:g.21806C>T
NG_032148.2:g.21806C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2655C>T	ENSP00000462607.2:p.Asp885=
ENST00000581729.2:c.2655C>T	ENSP00000462720.2:p.Asp885=
ENST00000581967.2:n.3107C>T
ENST00000583254.2:n.3704C>T
ENST00000699849.1:c.1758C>T	ENSP00000514647.1:p.Asp586=
ENST00000699850.1:n.1918C>T
ENST00000699851.1:n.2677C>T
ENST00000699852.1:c.*1331C>T	ENSP00000514648.1:n.*1331C>T
ENST00000699853.1:c.2655C>T	ENSP00000514649.1:p.Asp885=
ENST00000699854.1:n.2448C>T
ENST00000699855.1:n.3107C>T
ENST00000699856.1:c.2655C>T	ENSP00000514650.1:p.Asp885=
ENST00000699857.1:n.2663C>T
ENST00000699858.1:c.*1268C>T	ENSP00000514651.1:n.*1268C>T
ENST00000699859.1:c.2526C>T	ENSP00000514652.1:p.Asp842=
ENST00000699860.1:n.581+436C>T
ENST00000699861.1:n.2677C>T
ENST00000699862.1:n.3615C>T
ENST00000449476.7:c.2550C>T	ENSP00000396018.2:p.Asp850=
ENST00000581671.2:n.2644C>T
ENST00000643543.1:c.*1362C>T	ENSP00000494323.1:n.*1362C>T
ENST00000651323.1:c.2655C>T MANE Select	ENSP00000498499.1:p.Asp885=
ENST00000315684.12:c.2655C>T	ENSP00000313759.8:p.Asp885=
ENST00000449476.6:c.2550C>T	ENSP00000396018.2:p.Asp850=
ENST00000578240.1:n.883C>T
ENST00000578441.5:n.156C>T
ENST00000578537.1:c.371+436C>T
NM_025099.5:c.2655C>T	NP_079375.3:p.Asp885=
NR_046431.1:n.2609C>T
XM_006721577.2:c.2526C>T	XP_006721640.1:p.Asp842=
XM_006721578.2:c.2655C>T	XP_006721641.1:p.Asp885=
XM_006721579.2:c.2655C>T	XP_006721642.1:p.Asp885=
XM_011524010.1:c.2550C>T	XP_011522312.1:p.Asp850=
XM_011524011.1:c.1758C>T	XP_011522313.1:p.Asp586=
XR_429823.2:n.2698C>T
XR_429824.2:n.2698C>T
XR_429825.1:n.2518+436C>T
NM_025099.6:c.2655C>T MANE Select	NP_079375.3:p.Asp885=
XM_006721577.3:c.2526C>T	XP_006721640.1:p.Asp842=
XM_006721578.3:c.2655C>T	XP_006721641.1:p.Asp885=
XM_011524010.2:c.2550C>T	XP_011522312.1:p.Asp850=
XM_011524011.2:c.1758C>T	XP_011522313.1:p.Asp586=
XR_001752639.1:n.2569C>T
XR_001752640.1:n.2698C>T
XR_001752641.1:n.2698C>T
XR_001752642.1:n.2518+436C>T
XR_001752643.1:n.3128C>T
XR_002958073.1:n.2518+436C>T
XR_429823.3:n.2698C>T
XR_429824.3:n.2698C>T
NR_046431.2:n.2570C>T