Canonical Allele Identifier: CA397975440

Gene: CTC1

Linked Data

• COSMIC: COSM6148329
• MyVariant Identifiers: chr17:g.8134633G>C (hg19) ; chr17:g.8231315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231315G>C , CM000679.2:g.8231315G>C	GRCh38
NC_000017.10:g.8134633G>C , CM000679.1:g.8134633G>C	GRCh37
NC_000017.9:g.8075358G>C	NCBI36
NG_032148.1:g.21781C>G
NG_032148.2:g.21781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2630C>G	ENSP00000462607.2:p.Ser877Ter
ENST00000581729.2:c.2630C>G	ENSP00000462720.2:p.Ser877Ter
ENST00000581967.2:n.3082C>G
ENST00000583254.2:n.3679C>G
ENST00000699849.1:c.1733C>G	ENSP00000514647.1:p.Ser578Ter
ENST00000699850.1:n.1893C>G
ENST00000699851.1:n.2652C>G
ENST00000699852.1:c.*1306C>G	ENSP00000514648.1:n.*1306C>G
ENST00000699853.1:c.2630C>G	ENSP00000514649.1:p.Ser877Ter
ENST00000699854.1:n.2423C>G
ENST00000699855.1:n.3082C>G
ENST00000699856.1:c.2630C>G	ENSP00000514650.1:p.Ser877Ter
ENST00000699857.1:n.2638C>G
ENST00000699858.1:c.*1243C>G	ENSP00000514651.1:n.*1243C>G
ENST00000699859.1:c.2501C>G	ENSP00000514652.1:p.Ser834Ter
ENST00000699860.1:n.581+411C>G
ENST00000699861.1:n.2652C>G
ENST00000699862.1:n.3590C>G
ENST00000449476.7:c.2525C>G	ENSP00000396018.2:p.Ser842Ter
ENST00000581671.2:n.2619C>G
ENST00000643543.1:c.*1337C>G	ENSP00000494323.1:n.*1337C>G
ENST00000651323.1:c.2630C>G MANE Select	ENSP00000498499.1:p.Ser877Ter
ENST00000315684.12:c.2630C>G	ENSP00000313759.8:p.Ser877Ter
ENST00000449476.6:c.2525C>G	ENSP00000396018.2:p.Ser842Ter
ENST00000578240.1:n.858C>G
ENST00000578441.5:n.131C>G
ENST00000578537.1:c.371+411C>G
NM_025099.5:c.2630C>G	NP_079375.3:p.Ser877Ter
NR_046431.1:n.2584C>G
XM_006721577.2:c.2501C>G	XP_006721640.1:p.Ser834Ter
XM_006721578.2:c.2630C>G	XP_006721641.1:p.Ser877Ter
XM_006721579.2:c.2630C>G	XP_006721642.1:p.Ser877Ter
XM_011524010.1:c.2525C>G	XP_011522312.1:p.Ser842Ter
XM_011524011.1:c.1733C>G	XP_011522313.1:p.Ser578Ter
XR_429823.2:n.2673C>G
XR_429824.2:n.2673C>G
XR_429825.1:n.2518+411C>G
NM_025099.6:c.2630C>G MANE Select	NP_079375.3:p.Ser877Ter
XM_006721577.3:c.2501C>G	XP_006721640.1:p.Ser834Ter
XM_006721578.3:c.2630C>G	XP_006721641.1:p.Ser877Ter
XM_011524010.2:c.2525C>G	XP_011522312.1:p.Ser842Ter
XM_011524011.2:c.1733C>G	XP_011522313.1:p.Ser578Ter
XR_001752639.1:n.2544C>G
XR_001752640.1:n.2673C>G
XR_001752641.1:n.2673C>G
XR_001752642.1:n.2518+411C>G
XR_001752643.1:n.3103C>G
XR_002958073.1:n.2518+411C>G
XR_429823.3:n.2673C>G
XR_429824.3:n.2673C>G
NR_046431.2:n.2545C>G