Canonical Allele Identifier: CA397978358

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8135405A>G (hg19) ; chr17:g.8232087A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232087A>G , CM000679.2:g.8232087A>G	GRCh38
NC_000017.10:g.8135405A>G , CM000679.1:g.8135405A>G	GRCh37
NC_000017.9:g.8076130A>G	NCBI36
NG_032148.1:g.21009T>C
NG_032148.2:g.21009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2201T>C	ENSP00000462607.2:p.Leu734Ser
ENST00000581729.2:c.2201T>C	ENSP00000462720.2:p.Leu734Ser
ENST00000581967.2:n.2653T>C
ENST00000583254.2:n.2907T>C
ENST00000699849.1:c.1304T>C	ENSP00000514647.1:p.Leu435Ser
ENST00000699850.1:n.1464T>C
ENST00000699851.1:n.2223T>C
ENST00000699852.1:c.*877T>C	ENSP00000514648.1:n.*877T>C
ENST00000699853.1:c.2201T>C	ENSP00000514649.1:p.Leu734Ser
ENST00000699854.1:n.1994T>C
ENST00000699855.1:n.2653T>C
ENST00000699856.1:c.2201T>C	ENSP00000514650.1:p.Leu734Ser
ENST00000699857.1:n.2209T>C
ENST00000699858.1:c.*814T>C	ENSP00000514651.1:n.*814T>C
ENST00000699859.1:c.2072T>C	ENSP00000514652.1:p.Leu691Ser
ENST00000699860.1:n.307T>C
ENST00000699861.1:n.2223T>C
ENST00000699862.1:n.3161T>C
ENST00000449476.7:c.2096T>C	ENSP00000396018.2:p.Leu699Ser
ENST00000581671.2:n.2190T>C
ENST00000643543.1:c.*908T>C	ENSP00000494323.1:n.*908T>C
ENST00000651323.1:c.2201T>C MANE Select	ENSP00000498499.1:p.Leu734Ser
ENST00000315684.12:c.2201T>C	ENSP00000313759.8:p.Leu734Ser
ENST00000449476.6:c.2096T>C	ENSP00000396018.2:p.Leu699Ser
ENST00000578240.1:n.429T>C
ENST00000578537.1:c.97T>C
NM_025099.5:c.2201T>C	NP_079375.3:p.Leu734Ser
NR_046431.1:n.2155T>C
XM_006721577.2:c.2072T>C	XP_006721640.1:p.Leu691Ser
XM_006721578.2:c.2201T>C	XP_006721641.1:p.Leu734Ser
XM_006721579.2:c.2201T>C	XP_006721642.1:p.Leu734Ser
XM_011524010.1:c.2096T>C	XP_011522312.1:p.Leu699Ser
XM_011524011.1:c.1304T>C	XP_011522313.1:p.Leu435Ser
XR_429823.2:n.2244T>C
XR_429824.2:n.2244T>C
XR_429825.1:n.2244T>C
NM_025099.6:c.2201T>C MANE Select	NP_079375.3:p.Leu734Ser
XM_006721577.3:c.2072T>C	XP_006721640.1:p.Leu691Ser
XM_006721578.3:c.2201T>C	XP_006721641.1:p.Leu734Ser
XM_011524010.2:c.2096T>C	XP_011522312.1:p.Leu699Ser
XM_011524011.2:c.1304T>C	XP_011522313.1:p.Leu435Ser
XR_001752639.1:n.2115T>C
XR_001752640.1:n.2244T>C
XR_001752641.1:n.2244T>C
XR_001752642.1:n.2244T>C
XR_001752643.1:n.2674T>C
XR_002958073.1:n.2244T>C
XR_429823.3:n.2244T>C
XR_429824.3:n.2244T>C
NR_046431.2:n.2116T>C