Canonical Allele Identifier: CA2673056533

Gene: TERT

Linked Data

• gnomAD v4: 5-1260396-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260397_1260398insAC , CM000667.2:g.1260397_1260398insAC	GRCh38
NC_000005.9:g.1260512_1260513insAC , CM000667.1:g.1260512_1260513insAC	GRCh37
NC_000005.8:g.1313512_1313513insAC	NCBI36
NG_009265.1:g.39651_39652insTG , LRG_343:g.39651_39652insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+77_2970+78insTG MANE Select	ENSP00000309572.5:n.2970+77_2970+78insTG
ENST00000656021.1:c.*2516+77_*2516+78insTG	ENSP00000499759.1:n.*2516+77_*2516+78insTG
ENST00000667927.1:n.258+77_258+78insTG
ENST00000310581.9:c.2970+77_2970+78insTG	ENSP00000309572.5:n.2970+77_2970+78insTG
ENST00000334602.10:c.2781+77_2781+78insTG	ENSP00000334346.6:n.2781+77_2781+78insTG
ENST00000460137.6:c.2563+77_2563+78insTG	ENSP00000425003.1:n.2563+77_2563+78insTG
ENST00000484238.6:n.1412+77_1412+78insTG
NM_001193376.1:c.2781+77_2781+78insTG	NP_001180305.1:n.2781+77_2781+78insTG
NM_198253.2:c.2970+77_2970+78insTG , LRG_343t1:c.2970+77_2970+78insTG	NP_937983.2:n.2970+77_2970+78insTG
XM_011514104.1:c.1440+77_1440+78insTG	XP_011512406.1:n.1440+77_1440+78insTG
XM_011514105.1:c.1326+77_1326+78insTG	XP_011512407.1:n.1326+77_1326+78insTG
XM_011514106.1:c.1326+77_1326+78insTG	XP_011512408.1:n.1326+77_1326+78insTG
NR_149162.1:n.2657+77_2657+78insTG
NR_149163.1:n.2621+77_2621+78insTG
NM_001193376.2:c.2781+77_2781+78insTG	NP_001180305.1:n.2781+77_2781+78insTG
NM_198253.3:c.2970+77_2970+78insTG MANE Select	NP_937983.2:n.2970+77_2970+78insTG
NR_149162.2:n.2678+77_2678+78insTG
NR_149163.2:n.2642+77_2642+78insTG
NM_001193376.3:c.2781+77_2781+78insTG	NP_001180305.1:n.2781+77_2781+78insTG
NR_149162.3:n.2678+77_2678+78insTG
NR_149163.3:n.2642+77_2642+78insTG