Canonical Allele Identifier: CA1522582236

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293309_1293310delinsTC , CM000667.2:g.1293309_1293310delinsTC	GRCh38
NC_000005.9:g.1293424_1293425delinsTC , CM000667.1:g.1293424_1293425delinsTC	GRCh37
NC_000005.8:g.1346424_1346425delinsTC	NCBI36
NG_009265.1:g.6738_6739delinsGA , LRG_343:g.6738_6739delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1573+3_1573+4delinsGA MANE Select	ENSP00000309572.5:n.1573+3_1573+4delinsGA
ENST00000656021.1:c.1576_1577delinsGA	ENSP00000499759.1:p.Glu526=
ENST00000310581.9:c.1573+3_1573+4delinsGA	ENSP00000309572.5:n.1573+3_1573+4delinsGA
ENST00000334602.10:c.1573+3_1573+4delinsGA	ENSP00000334346.6:n.1573+3_1573+4delinsGA
ENST00000460137.6:c.1573+3_1573+4delinsGA	ENSP00000425003.1:n.1573+3_1573+4delinsGA
ENST00000508104.2:c.1573+3_1573+4delinsGA	ENSP00000426042.2:n.1573+3_1573+4delinsGA
NM_001193376.1:c.1573+3_1573+4delinsGA	NP_001180305.1:n.1573+3_1573+4delinsGA
NM_198253.2:c.1573+3_1573+4delinsGA , LRG_343t1:c.1573+3_1573+4delinsGA	NP_937983.2:n.1573+3_1573+4delinsGA
NR_149162.1:n.1631+3_1631+4delinsGA
NR_149163.1:n.1631+3_1631+4delinsGA
NM_001193376.2:c.1573+3_1573+4delinsGA	NP_001180305.1:n.1573+3_1573+4delinsGA
NM_198253.3:c.1573+3_1573+4delinsGA MANE Select	NP_937983.2:n.1573+3_1573+4delinsGA
NR_149162.2:n.1652+3_1652+4delinsGA
NR_149163.2:n.1652+3_1652+4delinsGA
NM_001193376.3:c.1573+3_1573+4delinsGA	NP_001180305.1:n.1573+3_1573+4delinsGA
NR_149162.3:n.1652+3_1652+4delinsGA
NR_149163.3:n.1652+3_1652+4delinsGA