Canonical Allele Identifier: CA497958737

Gene: CTC1

Linked Data

• ClinVar Variation Id: 1099132
• ClinVar RCV Id: RCV001421331
• dbSNP Id: rs2151508201
• MyVariant Identifiers: chr17:g.8135053A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231735A>G , CM000679.2:g.8231735A>G	GRCh38
NC_000017.10:g.8135053A>G , CM000679.1:g.8135053A>G	GRCh37
NC_000017.9:g.8075778A>G	NCBI36
NG_032148.1:g.21361T>C
NG_032148.2:g.21361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2466T>C	ENSP00000462607.2:p.Pro822=
ENST00000581729.2:c.2466T>C	ENSP00000462720.2:p.Pro822=
ENST00000581967.2:n.2918T>C
ENST00000583254.2:n.3259T>C
ENST00000699849.1:c.1569T>C	ENSP00000514647.1:p.Pro523=
ENST00000699850.1:n.1729T>C
ENST00000699851.1:n.2488T>C
ENST00000699852.1:c.*1142T>C	ENSP00000514648.1:n.*1142T>C
ENST00000699853.1:c.2466T>C	ENSP00000514649.1:p.Pro822=
ENST00000699854.1:n.2259T>C
ENST00000699855.1:n.2918T>C
ENST00000699856.1:c.2466T>C	ENSP00000514650.1:p.Pro822=
ENST00000699857.1:n.2474T>C
ENST00000699858.1:c.*1079T>C	ENSP00000514651.1:n.*1079T>C
ENST00000699859.1:c.2337T>C	ENSP00000514652.1:p.Pro779=
ENST00000699860.1:n.572T>C
ENST00000699861.1:n.2488T>C
ENST00000699862.1:n.3426T>C
ENST00000449476.7:c.2361T>C	ENSP00000396018.2:p.Pro787=
ENST00000581671.2:n.2455T>C
ENST00000643543.1:c.*1173T>C	ENSP00000494323.1:n.*1173T>C
ENST00000651323.1:c.2466T>C MANE Select	ENSP00000498499.1:p.Pro822=
ENST00000315684.12:c.2466T>C	ENSP00000313759.8:p.Pro822=
ENST00000449476.6:c.2361T>C	ENSP00000396018.2:p.Pro787=
ENST00000578240.1:n.694T>C
ENST00000578537.1:c.362T>C
NM_025099.5:c.2466T>C	NP_079375.3:p.Pro822=
NR_046431.1:n.2420T>C
XM_006721577.2:c.2337T>C	XP_006721640.1:p.Pro779=
XM_006721578.2:c.2466T>C	XP_006721641.1:p.Pro822=
XM_006721579.2:c.2466T>C	XP_006721642.1:p.Pro822=
XM_011524010.1:c.2361T>C	XP_011522312.1:p.Pro787=
XM_011524011.1:c.1569T>C	XP_011522313.1:p.Pro523=
XR_429823.2:n.2509T>C
XR_429824.2:n.2509T>C
XR_429825.1:n.2509T>C
NM_025099.6:c.2466T>C MANE Select	NP_079375.3:p.Pro822=
XM_006721577.3:c.2337T>C	XP_006721640.1:p.Pro779=
XM_006721578.3:c.2466T>C	XP_006721641.1:p.Pro822=
XM_011524010.2:c.2361T>C	XP_011522312.1:p.Pro787=
XM_011524011.2:c.1569T>C	XP_011522313.1:p.Pro523=
XR_001752639.1:n.2380T>C
XR_001752640.1:n.2509T>C
XR_001752641.1:n.2509T>C
XR_001752642.1:n.2509T>C
XR_001752643.1:n.2939T>C
XR_002958073.1:n.2509T>C
XR_429823.3:n.2509T>C
XR_429824.3:n.2509T>C
NR_046431.2:n.2381T>C