Canonical Allele Identifier: CA2673056465

Gene: TERT

Linked Data

• gnomAD v4: 5-1260354-GCAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260355_1260357del , CM000667.2:g.1260355_1260357del	GRCh38
NC_000005.9:g.1260470_1260472del , CM000667.1:g.1260470_1260472del	GRCh37
NC_000005.8:g.1313470_1313472del	NCBI36
NG_009265.1:g.39691_39693del , LRG_343:g.39691_39693del

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+117_2970+119del MANE Select	ENSP00000309572.5:n.2970+117_2970+119del
ENST00000656021.1:c.*2516+117_*2516+119del	ENSP00000499759.1:n.*2516+117_*2516+119del
ENST00000667927.1:n.258+117_258+119del
ENST00000310581.9:c.2970+117_2970+119del	ENSP00000309572.5:n.2970+117_2970+119del
ENST00000334602.10:c.2781+117_2781+119del	ENSP00000334346.6:n.2781+117_2781+119del
ENST00000460137.6:c.2563+117_2563+119del	ENSP00000425003.1:n.2563+117_2563+119del
ENST00000484238.6:n.1412+117_1412+119del
NM_001193376.1:c.2781+117_2781+119del	NP_001180305.1:n.2781+117_2781+119del
NM_198253.2:c.2970+117_2970+119del , LRG_343t1:c.2970+117_2970+119del	NP_937983.2:n.2970+117_2970+119del
XM_011514104.1:c.1440+117_1440+119del	XP_011512406.1:n.1440+117_1440+119del
XM_011514105.1:c.1326+117_1326+119del	XP_011512407.1:n.1326+117_1326+119del
XM_011514106.1:c.1326+117_1326+119del	XP_011512408.1:n.1326+117_1326+119del
NR_149162.1:n.2657+117_2657+119del
NR_149163.1:n.2621+117_2621+119del
NM_001193376.2:c.2781+117_2781+119del	NP_001180305.1:n.2781+117_2781+119del
NM_198253.3:c.2970+117_2970+119del MANE Select	NP_937983.2:n.2970+117_2970+119del
NR_149162.2:n.2678+117_2678+119del
NR_149163.2:n.2642+117_2642+119del
NM_001193376.3:c.2781+117_2781+119del	NP_001180305.1:n.2781+117_2781+119del
NR_149162.3:n.2678+117_2678+119del
NR_149163.3:n.2642+117_2642+119del