Canonical Allele Identifier: CA397975537

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8134646C>G (hg19) ; chr17:g.8231328C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231328C>G , CM000679.2:g.8231328C>G	GRCh38
NC_000017.10:g.8134646C>G , CM000679.1:g.8134646C>G	GRCh37
NC_000017.9:g.8075371C>G	NCBI36
NG_032148.1:g.21768G>C
NG_032148.2:g.21768G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000580299.2:c.2617G>C	ENSP00000462607.2:p.Asp873His
ENST00000581729.2:c.2617G>C	ENSP00000462720.2:p.Asp873His
ENST00000581967.2:n.3069G>C
ENST00000583254.2:n.3666G>C
ENST00000699849.1:c.1720G>C	ENSP00000514647.1:p.Asp574His
ENST00000699850.1:n.1880G>C
ENST00000699851.1:n.2639G>C
ENST00000699852.1:c.*1293G>C	ENSP00000514648.1:n.*1293G>C
ENST00000699853.1:c.2617G>C	ENSP00000514649.1:p.Asp873His
ENST00000699854.1:n.2410G>C
ENST00000699855.1:n.3069G>C
ENST00000699856.1:c.2617G>C	ENSP00000514650.1:p.Asp873His
ENST00000699857.1:n.2625G>C
ENST00000699858.1:c.*1230G>C	ENSP00000514651.1:n.*1230G>C
ENST00000699859.1:c.2488G>C	ENSP00000514652.1:p.Asp830His
ENST00000699860.1:n.581+398G>C
ENST00000699861.1:n.2639G>C
ENST00000699862.1:n.3577G>C
ENST00000449476.7:c.2512G>C	ENSP00000396018.2:p.Asp838His
ENST00000581671.2:n.2606G>C
ENST00000643543.1:c.*1324G>C	ENSP00000494323.1:n.*1324G>C
ENST00000651323.1:c.2617G>C MANE Select	ENSP00000498499.1:p.Asp873His
ENST00000315684.12:c.2617G>C	ENSP00000313759.8:p.Asp873His
ENST00000449476.6:c.2512G>C	ENSP00000396018.2:p.Asp838His
ENST00000578240.1:n.845G>C
ENST00000578441.5:n.118G>C
ENST00000578537.1:c.371+398G>C
NM_025099.5:c.2617G>C	NP_079375.3:p.Asp873His
NR_046431.1:n.2571G>C
XM_006721577.2:c.2488G>C	XP_006721640.1:p.Asp830His
XM_006721578.2:c.2617G>C	XP_006721641.1:p.Asp873His
XM_006721579.2:c.2617G>C	XP_006721642.1:p.Asp873His
XM_011524010.1:c.2512G>C	XP_011522312.1:p.Asp838His
XM_011524011.1:c.1720G>C	XP_011522313.1:p.Asp574His
XR_429823.2:n.2660G>C
XR_429824.2:n.2660G>C
XR_429825.1:n.2518+398G>C
NM_025099.6:c.2617G>C MANE Select	NP_079375.3:p.Asp873His
XM_006721577.3:c.2488G>C	XP_006721640.1:p.Asp830His
XM_006721578.3:c.2617G>C	XP_006721641.1:p.Asp873His
XM_011524010.2:c.2512G>C	XP_011522312.1:p.Asp838His
XM_011524011.2:c.1720G>C	XP_011522313.1:p.Asp574His
XR_001752639.1:n.2531G>C
XR_001752640.1:n.2660G>C
XR_001752641.1:n.2660G>C
XR_001752642.1:n.2518+398G>C
XR_001752643.1:n.3090G>C
XR_002958073.1:n.2518+398G>C
XR_429823.3:n.2660G>C
XR_429824.3:n.2660G>C
NR_046431.2:n.2532G>C