Canonical Allele Identifier: CA1522559114

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294877_1294878delinsAG , CM000667.2:g.1294877_1294878delinsAG	GRCh38
NC_000005.9:g.1294992_1294993delinsAG , CM000667.1:g.1294992_1294993delinsAG	GRCh37
NC_000005.8:g.1347992_1347993delinsAG	NCBI36
NG_009265.1:g.5170_5171delinsCT , LRG_343:g.5170_5171delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.112_113delinsCT MANE Select	ENSP00000309572.5:p.Leu38=
ENST00000656021.1:c.112_113delinsCT	ENSP00000499759.1:p.Leu38=
ENST00000310581.9:c.112_113delinsCT	ENSP00000309572.5:p.Leu38=
ENST00000334602.10:c.112_113delinsCT	ENSP00000334346.6:p.Leu38=
ENST00000460137.6:c.112_113delinsCT	ENSP00000425003.1:p.Leu38=
ENST00000508104.2:c.112_113delinsCT	ENSP00000426042.2:p.Leu38=
ENST00000522877.1:n.192_193delinsCT
NM_001193376.1:c.112_113delinsCT	NP_001180305.1:p.Leu38=
NM_198253.2:c.112_113delinsCT , LRG_343t1:c.112_113delinsCT	NP_937983.2:p.Leu38=
NR_149162.1:n.170_171delinsCT
NR_149163.1:n.170_171delinsCT
NM_001193376.2:c.112_113delinsCT	NP_001180305.1:p.Leu38=
NM_198253.3:c.112_113delinsCT MANE Select	NP_937983.2:p.Leu38=
NR_149162.2:n.191_192delinsCT
NR_149163.2:n.191_192delinsCT
NM_001193376.3:c.112_113delinsCT	NP_001180305.1:p.Leu38=
NR_149162.3:n.191_192delinsCT
NR_149163.3:n.191_192delinsCT