Canonical Allele Identifier: CA1522539587

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260321_1260325delinsCATGT , CM000667.2:g.1260321_1260325delinsCATGT	GRCh38
NC_000005.9:g.1260436_1260440delinsCATGT , CM000667.1:g.1260436_1260440delinsCATGT	GRCh37
NC_000005.8:g.1313436_1313440delinsCATGT	NCBI36
NG_009265.1:g.39723_39727delinsACATG , LRG_343:g.39723_39727delinsACATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+149_2970+153delinsACATG MANE Select	ENSP00000309572.5:n.2970+149_2970+153delinsACATG
ENST00000656021.1:c.*2516+149_*2516+153delinsACATG	ENSP00000499759.1:n.*2516+149_*2516+153delinsACATG
ENST00000667927.1:n.258+149_258+153delinsACATG
ENST00000310581.9:c.2970+149_2970+153delinsACATG	ENSP00000309572.5:n.2970+149_2970+153delinsACATG
ENST00000334602.10:c.2781+149_2781+153delinsACATG	ENSP00000334346.6:n.2781+149_2781+153delinsACATG
ENST00000460137.6:c.2563+149_2563+153delinsACATG	ENSP00000425003.1:n.2563+149_2563+153delinsACATG
ENST00000484238.6:n.1412+149_1412+153delinsACATG
NM_001193376.1:c.2781+149_2781+153delinsACATG	NP_001180305.1:n.2781+149_2781+153delinsACATG
NM_198253.2:c.2970+149_2970+153delinsACATG , LRG_343t1:c.2970+149_2970+153delinsACATG	NP_937983.2:n.2970+149_2970+153delinsACATG
XM_011514104.1:c.1440+149_1440+153delinsACATG	XP_011512406.1:n.1440+149_1440+153delinsACATG
XM_011514105.1:c.1326+149_1326+153delinsACATG	XP_011512407.1:n.1326+149_1326+153delinsACATG
XM_011514106.1:c.1326+149_1326+153delinsACATG	XP_011512408.1:n.1326+149_1326+153delinsACATG
NR_149162.1:n.2657+149_2657+153delinsACATG
NR_149163.1:n.2621+149_2621+153delinsACATG
NM_001193376.2:c.2781+149_2781+153delinsACATG	NP_001180305.1:n.2781+149_2781+153delinsACATG
NM_198253.3:c.2970+149_2970+153delinsACATG MANE Select	NP_937983.2:n.2970+149_2970+153delinsACATG
NR_149162.2:n.2678+149_2678+153delinsACATG
NR_149163.2:n.2642+149_2642+153delinsACATG
NM_001193376.3:c.2781+149_2781+153delinsACATG	NP_001180305.1:n.2781+149_2781+153delinsACATG
NR_149162.3:n.2678+149_2678+153delinsACATG
NR_149163.3:n.2642+149_2642+153delinsACATG