Canonical Allele Identifier: CA645372763

Gene: TERT

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294549dup , CM000667.2:g.1294549dup	GRCh38
NC_000005.9:g.1294664dup , CM000667.1:g.1294664dup	GRCh37
NC_000005.8:g.1347664dup	NCBI36
NG_009265.1:g.5499dup , LRG_343:g.5499dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.337dup MANE Select	ENSP00000309572.5:p.Glu113GlyfsTer?
ENST00000656021.1:c.337dup	ENSP00000499759.1:p.Glu113GlyfsTer?
ENST00000310581.9:c.337dup	ENSP00000309572.5:p.Glu113GlyfsTer?
ENST00000334602.10:c.337dup	ENSP00000334346.6:p.Glu113GlyfsTer?
ENST00000460137.6:c.337dup	ENSP00000425003.1:p.Glu113GlyfsTer?
ENST00000508104.2:c.337dup	ENSP00000426042.2:p.Glu113GlyfsTer?
NM_001193376.1:c.337dup	NP_001180305.1:p.Glu113GlyfsTer?
NM_198253.2:c.337dup , LRG_343t1:c.337dup	NP_937983.2:p.Glu113GlyfsTer?
NR_149162.1:n.395dup
NR_149163.1:n.395dup
NM_001193376.2:c.337dup	NP_001180305.1:p.Glu113GlyfsTer?
NM_198253.3:c.337dup MANE Select	NP_937983.2:p.Glu113GlyfsTer?
NR_149162.2:n.416dup
NR_149163.2:n.416dup
NM_001193376.3:c.337dup	NP_001180305.1:p.Glu113GlyfsTer?
NR_149162.3:n.416dup
NR_149163.3:n.416dup