Canonical Allele Identifier: CA8372206

Gene: CTC1

Linked Data

• ClinVar Variation Id: 698521
• ClinVar RCV Id: RCV001440274
• dbSNP Id: rs755004377
• ExAC: 17:8135747 G / A
• gnomAD v2: 17-8135747-G-A
• gnomAD v3: 17-8232429-G-A
• gnomAD v4: 17-8232429-G-A
• MyVariant Identifiers: chr17:g.8135747G>A (hg19) ; chr17:g.8232429G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232429G>A , CM000679.2:g.8232429G>A	GRCh38
NC_000017.10:g.8135747G>A , CM000679.1:g.8135747G>A	GRCh37
NC_000017.9:g.8076472G>A	NCBI36
NG_032148.1:g.20667C>T
NG_032148.2:g.20667C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000580299.2:c.1992C>T	ENSP00000462607.2:p.Asp664=
ENST00000581729.2:c.1992C>T	ENSP00000462720.2:p.Asp664=
ENST00000581967.2:n.2444C>T
ENST00000583254.2:n.2698C>T
ENST00000699849.1:c.1095C>T	ENSP00000514647.1:p.Asp365=
ENST00000699850.1:n.1255C>T
ENST00000699851.1:n.2014C>T
ENST00000699852.1:c.*668C>T	ENSP00000514648.1:n.*668C>T
ENST00000699853.1:c.1992C>T	ENSP00000514649.1:p.Asp664=
ENST00000699854.1:n.1785C>T
ENST00000699855.1:n.2444C>T
ENST00000699856.1:c.1992C>T	ENSP00000514650.1:p.Asp664=
ENST00000699857.1:n.2000C>T
ENST00000699858.1:c.*605C>T	ENSP00000514651.1:n.*605C>T
ENST00000699859.1:c.1863C>T	ENSP00000514652.1:p.Asp621=
ENST00000699860.1:n.98C>T
ENST00000699861.1:n.2014C>T
ENST00000699862.1:n.2952C>T
ENST00000449476.7:c.1887C>T	ENSP00000396018.2:p.Asp629=
ENST00000581671.2:n.1981C>T
ENST00000643543.1:c.*699C>T	ENSP00000494323.1:n.*699C>T
ENST00000651323.1:c.1992C>T MANE Select	ENSP00000498499.1:p.Asp664=
ENST00000315684.12:c.1992C>T	ENSP00000313759.8:p.Asp664=
ENST00000449476.6:c.1887C>T	ENSP00000396018.2:p.Asp629=
ENST00000578240.1:n.220C>T
NM_025099.5:c.1992C>T	NP_079375.3:p.Asp664=
NR_046431.1:n.1946C>T
XM_006721577.2:c.1863C>T	XP_006721640.1:p.Asp621=
XM_006721578.2:c.1992C>T	XP_006721641.1:p.Asp664=
XM_006721579.2:c.1992C>T	XP_006721642.1:p.Asp664=
XM_011524010.1:c.1887C>T	XP_011522312.1:p.Asp629=
XM_011524011.1:c.1095C>T	XP_011522313.1:p.Asp365=
XR_429823.2:n.2035C>T
XR_429824.2:n.2035C>T
XR_429825.1:n.2035C>T
NM_025099.6:c.1992C>T MANE Select	NP_079375.3:p.Asp664=
XM_006721577.3:c.1863C>T	XP_006721640.1:p.Asp621=
XM_006721578.3:c.1992C>T	XP_006721641.1:p.Asp664=
XM_011524010.2:c.1887C>T	XP_011522312.1:p.Asp629=
XM_011524011.2:c.1095C>T	XP_011522313.1:p.Asp365=
XR_001752639.1:n.1906C>T
XR_001752640.1:n.2035C>T
XR_001752641.1:n.2035C>T
XR_001752642.1:n.2035C>T
XR_001752643.1:n.2465C>T
XR_001752644.1:n.2321C>T
XR_002958073.1:n.2035C>T
XR_429823.3:n.2035C>T
XR_429824.3:n.2035C>T
NR_046431.2:n.1907C>T