Canonical Allele Identifier: CA8372041

Gene: CTC1

Linked Data

• ClinVar Variation Id: 412530
• ClinVar RCV Id: RCV000468366 ; RCV001726178
• dbSNP Id: rs146214808
• ExAC: 17:8134755 G / C
• gnomAD v2: 17-8134755-G-C
• gnomAD v3: 17-8231437-G-C
• gnomAD v4: 17-8231437-G-C
• MyVariant Identifiers: chr17:g.8134755G>C (hg19) ; chr17:g.8231437G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231437G>C , CM000679.2:g.8231437G>C	GRCh38
NC_000017.10:g.8134755G>C , CM000679.1:g.8134755G>C	GRCh37
NC_000017.9:g.8075480G>C	NCBI36
NG_032148.1:g.21659C>G
NG_032148.2:g.21659C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000580299.2:c.2508C>G	ENSP00000462607.2:p.Ser836=
ENST00000581729.2:c.2508C>G	ENSP00000462720.2:p.Ser836=
ENST00000581967.2:n.2960C>G
ENST00000583254.2:n.3557C>G
ENST00000699849.1:c.1611C>G	ENSP00000514647.1:p.Ser537=
ENST00000699850.1:n.1771C>G
ENST00000699851.1:n.2530C>G
ENST00000699852.1:c.*1184C>G	ENSP00000514648.1:n.*1184C>G
ENST00000699853.1:c.2508C>G	ENSP00000514649.1:p.Ser836=
ENST00000699854.1:n.2301C>G
ENST00000699855.1:n.2960C>G
ENST00000699856.1:c.2508C>G	ENSP00000514650.1:p.Ser836=
ENST00000699857.1:n.2516C>G
ENST00000699858.1:c.*1121C>G	ENSP00000514651.1:n.*1121C>G
ENST00000699859.1:c.2379C>G	ENSP00000514652.1:p.Ser793=
ENST00000699860.1:n.581+289C>G
ENST00000699861.1:n.2530C>G
ENST00000699862.1:n.3468C>G
ENST00000449476.7:c.2403C>G	ENSP00000396018.2:p.Ser801=
ENST00000581671.2:n.2497C>G
ENST00000643543.1:c.*1215C>G	ENSP00000494323.1:n.*1215C>G
ENST00000651323.1:c.2508C>G MANE Select	ENSP00000498499.1:p.Ser836=
ENST00000315684.12:c.2508C>G	ENSP00000313759.8:p.Ser836=
ENST00000449476.6:c.2403C>G	ENSP00000396018.2:p.Ser801=
ENST00000578240.1:n.736C>G
ENST00000578441.5:n.9C>G
ENST00000578537.1:c.371+289C>G
NM_025099.5:c.2508C>G	NP_079375.3:p.Ser836=
NR_046431.1:n.2462C>G
XM_006721577.2:c.2379C>G	XP_006721640.1:p.Ser793=
XM_006721578.2:c.2508C>G	XP_006721641.1:p.Ser836=
XM_006721579.2:c.2508C>G	XP_006721642.1:p.Ser836=
XM_011524010.1:c.2403C>G	XP_011522312.1:p.Ser801=
XM_011524011.1:c.1611C>G	XP_011522313.1:p.Ser537=
XR_429823.2:n.2551C>G
XR_429824.2:n.2551C>G
XR_429825.1:n.2518+289C>G
NM_025099.6:c.2508C>G MANE Select	NP_079375.3:p.Ser836=
XM_006721577.3:c.2379C>G	XP_006721640.1:p.Ser793=
XM_006721578.3:c.2508C>G	XP_006721641.1:p.Ser836=
XM_011524010.2:c.2403C>G	XP_011522312.1:p.Ser801=
XM_011524011.2:c.1611C>G	XP_011522313.1:p.Ser537=
XR_001752639.1:n.2422C>G
XR_001752640.1:n.2551C>G
XR_001752641.1:n.2551C>G
XR_001752642.1:n.2518+289C>G
XR_001752643.1:n.2981C>G
XR_002958073.1:n.2518+289C>G
XR_429823.3:n.2551C>G
XR_429824.3:n.2551C>G
NR_046431.2:n.2423C>G