Canonical Allele Identifier: CA497782713

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8140780A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8237462A>G , CM000679.2:g.8237462A>G	GRCh38
NC_000017.10:g.8140780A>G , CM000679.1:g.8140780A>G	GRCh37
NC_000017.9:g.8081505A>G	NCBI36
NG_032148.1:g.15634T>C
NG_032148.2:g.15634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.705T>C	ENSP00000462607.2:p.Ala235=
ENST00000581729.2:c.705T>C	ENSP00000462720.2:p.Ala235=
ENST00000581967.2:n.727T>C
ENST00000583254.2:n.119T>C
ENST00000699849.1:c.-193T>C	ENSP00000514647.1:n.-193T>C
ENST00000699850.1:n.56-1120T>C
ENST00000699851.1:n.727T>C
ENST00000699852.1:c.705T>C	ENSP00000514648.1:p.Ala235=
ENST00000699853.1:c.705T>C	ENSP00000514649.1:p.Ala235=
ENST00000699854.1:n.498T>C
ENST00000699855.1:n.727T>C
ENST00000699856.1:c.705T>C	ENSP00000514650.1:p.Ala235=
ENST00000699857.1:n.713T>C
ENST00000699858.1:c.705T>C	ENSP00000514651.1:p.Ala235=
ENST00000699859.1:c.705T>C	ENSP00000514652.1:p.Ala235=
ENST00000699861.1:n.727T>C
ENST00000699862.1:n.592T>C
ENST00000449476.7:c.648-48T>C	ENSP00000396018.2:n.648-48T>C
ENST00000581671.2:n.546T>C
ENST00000643543.1:c.705T>C	ENSP00000494323.1:p.Ala235=
ENST00000651323.1:c.705T>C MANE Select	ENSP00000498499.1:p.Ala235=
ENST00000315684.12:c.705T>C	ENSP00000313759.8:p.Ala235=
ENST00000449476.6:c.648-48T>C	ENSP00000396018.2:n.648-48T>C
ENST00000581671.1:n.546T>C
NM_025099.5:c.705T>C	NP_079375.3:p.Ala235=
NR_046431.1:n.707-48T>C
XM_006721577.2:c.705T>C	XP_006721640.1:p.Ala235=
XM_006721578.2:c.705T>C	XP_006721641.1:p.Ala235=
XM_006721579.2:c.705T>C	XP_006721642.1:p.Ala235=
XM_011524010.1:c.648-48T>C	XP_011522312.1:n.648-48T>C
XM_011524011.1:c.-197T>C	XP_011522313.1:n.-197T>C
XR_429823.2:n.748T>C
XR_429824.2:n.748T>C
XR_429825.1:n.748T>C
NM_025099.6:c.705T>C MANE Select	NP_079375.3:p.Ala235=
XM_006721577.3:c.705T>C	XP_006721640.1:p.Ala235=
XM_006721578.3:c.705T>C	XP_006721641.1:p.Ala235=
XM_011524010.2:c.648-48T>C	XP_011522312.1:n.648-48T>C
XM_011524011.2:c.-197T>C	XP_011522313.1:n.-197T>C
XR_001752639.1:n.748T>C
XR_001752640.1:n.748T>C
XR_001752641.1:n.748T>C
XR_001752642.1:n.748T>C
XR_001752643.1:n.748T>C
XR_001752644.1:n.748T>C
XR_002958073.1:n.748T>C
XR_429823.3:n.748T>C
XR_429824.3:n.748T>C
NR_046431.2:n.668-48T>C