Canonical Allele Identifier: CA2673080616

Gene: TERT

Linked Data

• gnomAD v4: 5-1293303-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293308_1293310del , CM000667.2:g.1293308_1293310del	GRCh38
NC_000005.9:g.1293423_1293425del , CM000667.1:g.1293423_1293425del	GRCh37
NC_000005.8:g.1346423_1346425del	NCBI36
NG_009265.1:g.6742_6744del , LRG_343:g.6742_6744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1573+7_1573+9del MANE Select	ENSP00000309572.5:n.1573+7_1573+9del
ENST00000656021.1:c.1580_1582del	ENSP00000499759.1:p.Glu527del
ENST00000310581.9:c.1573+7_1573+9del	ENSP00000309572.5:n.1573+7_1573+9del
ENST00000334602.10:c.1573+7_1573+9del	ENSP00000334346.6:n.1573+7_1573+9del
ENST00000460137.6:c.1573+7_1573+9del	ENSP00000425003.1:n.1573+7_1573+9del
ENST00000508104.2:c.1573+7_1573+9del	ENSP00000426042.2:n.1573+7_1573+9del
NM_001193376.1:c.1573+7_1573+9del	NP_001180305.1:n.1573+7_1573+9del
NM_198253.2:c.1573+7_1573+9del , LRG_343t1:c.1573+7_1573+9del	NP_937983.2:n.1573+7_1573+9del
NR_149162.1:n.1631+7_1631+9del
NR_149163.1:n.1631+7_1631+9del
NM_001193376.2:c.1573+7_1573+9del	NP_001180305.1:n.1573+7_1573+9del
NM_198253.3:c.1573+7_1573+9del MANE Select	NP_937983.2:n.1573+7_1573+9del
NR_149162.2:n.1652+7_1652+9del
NR_149163.2:n.1652+7_1652+9del
NM_001193376.3:c.1573+7_1573+9del	NP_001180305.1:n.1573+7_1573+9del
NR_149162.3:n.1652+7_1652+9del
NR_149163.3:n.1652+7_1652+9del