Canonical Allele Identifier: CA1522560624

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275762_1275772delinsCCCACAGATCT , CM000667.2:g.1275762_1275772delinsCCCACAGATCT	GRCh38
NC_000005.9:g.1275877_1275887delinsCCCACAGATCT , CM000667.1:g.1275877_1275887delinsCCCACAGATCT	GRCh37
NC_000005.8:g.1328877_1328887delinsCCCACAGATCT	NCBI36
NG_009265.1:g.24276_24286delinsAGATCTGTGGG , LRG_343:g.24276_24286delinsAGATCTGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2869_2286+2879delinsAGATCTGTGGG MANE Select	ENSP00000309572.5:n.2286+2869_2286+2879delinsAGATCTGTGGG
ENST00000656021.1:c.*1832+2869_*1832+2879delinsAGATCTGTGGG	ENSP00000499759.1:n.*1832+2869_*1832+2879delinsAGATCTGTGGG
ENST00000310581.9:c.2286+2869_2286+2879delinsAGATCTGTGGG	ENSP00000309572.5:n.2286+2869_2286+2879delinsAGATCTGTGGG
ENST00000334602.10:c.2286+2869_2286+2879delinsAGATCTGTGGG	ENSP00000334346.6:n.2286+2869_2286+2879delinsAGATCTGTGGG
ENST00000460137.6:c.2250+2869_2250+2879delinsAGATCTGTGGG	ENSP00000425003.1:n.2250+2869_2250+2879delinsAGATCTGTGGG
ENST00000484238.6:n.1099+2869_1099+2879delinsAGATCTGTGGG
ENST00000508104.2:c.2286+2869_2286+2879delinsAGATCTGTGGG	ENSP00000426042.2:n.2286+2869_2286+2879delinsAGATCTGTGGG
NM_001193376.1:c.2286+2869_2286+2879delinsAGATCTGTGGG	NP_001180305.1:n.2286+2869_2286+2879delinsAGATCTGTGGG
NM_198253.2:c.2286+2869_2286+2879delinsAGATCTGTGGG , LRG_343t1:c.2286+2869_2286+2879delinsAGATCTGTGGG	NP_937983.2:n.2286+2869_2286+2879delinsAGATCTGTGGG
XM_011514104.1:c.756+2869_756+2879delinsAGATCTGTGGG	XP_011512406.1:n.756+2869_756+2879delinsAGATCTGTGGG
XM_011514105.1:c.642+2869_642+2879delinsAGATCTGTGGG	XP_011512407.1:n.642+2869_642+2879delinsAGATCTGTGGG
XM_011514106.1:c.642+2869_642+2879delinsAGATCTGTGGG	XP_011512408.1:n.642+2869_642+2879delinsAGATCTGTGGG
NR_149162.1:n.2344+2869_2344+2879delinsAGATCTGTGGG
NR_149163.1:n.2308+2869_2308+2879delinsAGATCTGTGGG
NM_001193376.2:c.2286+2869_2286+2879delinsAGATCTGTGGG	NP_001180305.1:n.2286+2869_2286+2879delinsAGATCTGTGGG
NM_198253.3:c.2286+2869_2286+2879delinsAGATCTGTGGG MANE Select	NP_937983.2:n.2286+2869_2286+2879delinsAGATCTGTGGG
NR_149162.2:n.2365+2869_2365+2879delinsAGATCTGTGGG
NR_149163.2:n.2329+2869_2329+2879delinsAGATCTGTGGG
NM_001193376.3:c.2286+2869_2286+2879delinsAGATCTGTGGG	NP_001180305.1:n.2286+2869_2286+2879delinsAGATCTGTGGG
NR_149162.3:n.2365+2869_2365+2879delinsAGATCTGTGGG
NR_149163.3:n.2329+2869_2329+2879delinsAGATCTGTGGG