Canonical Allele Identifier: CA1522539833

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260518_1260520delinsCAA , CM000667.2:g.1260518_1260520delinsCAA	GRCh38
NC_000005.9:g.1260633_1260635delinsCAA , CM000667.1:g.1260633_1260635delinsCAA	GRCh37
NC_000005.8:g.1313633_1313635delinsCAA	NCBI36
NG_009265.1:g.39528_39530delinsTTG , LRG_343:g.39528_39530delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2924_2926delinsTTG MANE Select	ENSP00000309572.5:p.Phe975=
ENST00000656021.1:c.*2470_*2472delinsTTG	ENSP00000499759.1:n.*2470_*2472delinsTTG
ENST00000667927.1:n.212_214delinsTTG
ENST00000310581.9:c.2924_2926delinsTTG	ENSP00000309572.5:p.Phe975=
ENST00000334602.10:c.2735_2737delinsTTG	ENSP00000334346.6:p.Phe912=
ENST00000460137.6:c.2517_2519delinsTTG	ENSP00000425003.1:n.2517_2519delinsTTG
ENST00000484238.6:n.1366_1368delinsTTG
NM_001193376.1:c.2735_2737delinsTTG	NP_001180305.1:p.Phe912=
NM_198253.2:c.2924_2926delinsTTG , LRG_343t1:c.2924_2926delinsTTG	NP_937983.2:p.Phe975=
XM_011514104.1:c.1394_1396delinsTTG	XP_011512406.1:p.Phe465=
XM_011514105.1:c.1280_1282delinsTTG	XP_011512407.1:p.Phe427=
XM_011514106.1:c.1280_1282delinsTTG	XP_011512408.1:p.Phe427=
NR_149162.1:n.2611_2613delinsTTG
NR_149163.1:n.2575_2577delinsTTG
NM_001193376.2:c.2735_2737delinsTTG	NP_001180305.1:p.Phe912=
NM_198253.3:c.2924_2926delinsTTG MANE Select	NP_937983.2:p.Phe975=
NR_149162.2:n.2632_2634delinsTTG
NR_149163.2:n.2596_2598delinsTTG
NM_001193376.3:c.2735_2737delinsTTG	NP_001180305.1:p.Phe912=
NR_149162.3:n.2632_2634delinsTTG
NR_149163.3:n.2596_2598delinsTTG