Canonical Allele Identifier: CA2673080946

Gene: TERT

Linked Data

• gnomAD v4: 5-1294745-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294745_1294746insT , CM000667.2:g.1294745_1294746insT	GRCh38
NC_000005.9:g.1294860_1294861insT , CM000667.1:g.1294860_1294861insT	GRCh37
NC_000005.8:g.1347860_1347861insT	NCBI36
NG_009265.1:g.5302_5303insA , LRG_343:g.5302_5303insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.219+25_219+26insA MANE Select	ENSP00000309572.5:n.219+25_219+26insA
ENST00000656021.1:c.219+25_219+26insA	ENSP00000499759.1:n.219+25_219+26insA
ENST00000310581.9:c.219+25_219+26insA	ENSP00000309572.5:n.219+25_219+26insA
ENST00000334602.10:c.219+25_219+26insA	ENSP00000334346.6:n.219+25_219+26insA
ENST00000460137.6:c.219+25_219+26insA	ENSP00000425003.1:n.219+25_219+26insA
ENST00000508104.2:c.219+25_219+26insA	ENSP00000426042.2:n.219+25_219+26insA
ENST00000522877.1:n.299+25_299+26insA
NM_001193376.1:c.219+25_219+26insA	NP_001180305.1:n.219+25_219+26insA
NM_198253.2:c.219+25_219+26insA , LRG_343t1:c.219+25_219+26insA	NP_937983.2:n.219+25_219+26insA
NR_149162.1:n.277+25_277+26insA
NR_149163.1:n.277+25_277+26insA
NM_001193376.2:c.219+25_219+26insA	NP_001180305.1:n.219+25_219+26insA
NM_198253.3:c.219+25_219+26insA MANE Select	NP_937983.2:n.219+25_219+26insA
NR_149162.2:n.298+25_298+26insA
NR_149163.2:n.298+25_298+26insA
NM_001193376.3:c.219+25_219+26insA	NP_001180305.1:n.219+25_219+26insA
NR_149162.3:n.298+25_298+26insA
NR_149163.3:n.298+25_298+26insA