Canonical Allele Identifier: CA2673079535

Gene: TERT

Linked Data

• gnomAD v4: 5-1279525-CCCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1279528_1279531del , CM000667.2:g.1279528_1279531del	GRCh38
NC_000005.9:g.1279643_1279646del , CM000667.1:g.1279643_1279646del	GRCh37
NC_000005.8:g.1332643_1332646del	NCBI36
NG_009265.1:g.20519_20522del , LRG_343:g.20519_20522del

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.1951-59_1951-56del MANE Select	ENSP00000309572.5:n.1951-59_1951-56del
ENST00000656021.1:c.*1497-59_*1497-56del	ENSP00000499759.1:n.*1497-59_*1497-56del
ENST00000310581.9:c.1951-59_1951-56del	ENSP00000309572.5:n.1951-59_1951-56del
ENST00000334602.10:c.1951-59_1951-56del	ENSP00000334346.6:n.1951-59_1951-56del
ENST00000460137.6:c.1951-59_1951-56del	ENSP00000425003.1:n.1951-59_1951-56del
ENST00000484238.6:n.764-59_764-56del
ENST00000508104.2:c.1951-59_1951-56del	ENSP00000426042.2:n.1951-59_1951-56del
NM_001193376.1:c.1951-59_1951-56del	NP_001180305.1:n.1951-59_1951-56del
NM_198253.2:c.1951-59_1951-56del , LRG_343t1:c.1951-59_1951-56del	NP_937983.2:n.1951-59_1951-56del
XM_011514104.1:c.421-59_421-56del	XP_011512406.1:n.421-59_421-56del
XM_011514105.1:c.307-59_307-56del	XP_011512407.1:n.307-59_307-56del
XM_011514106.1:c.307-59_307-56del	XP_011512408.1:n.307-59_307-56del
NR_149162.1:n.2009-59_2009-56del
NR_149163.1:n.2009-59_2009-56del
NM_001193376.2:c.1951-59_1951-56del	NP_001180305.1:n.1951-59_1951-56del
NM_198253.3:c.1951-59_1951-56del MANE Select	NP_937983.2:n.1951-59_1951-56del
NR_149162.2:n.2030-59_2030-56del
NR_149163.2:n.2030-59_2030-56del
NM_001193376.3:c.1951-59_1951-56del	NP_001180305.1:n.1951-59_1951-56del
NR_149162.3:n.2030-59_2030-56del
NR_149163.3:n.2030-59_2030-56del