Canonical Allele Identifier: CA112947206

Gene: TERT

Linked Data

• dbSNP Id: rs202070680
• MyVariant Identifiers: chr5:g.1275879_1275887del (hg19) ; chr5:g.1275764_1275772del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275765_1275773del , CM000667.2:g.1275765_1275773del	GRCh38
NC_000005.9:g.1275880_1275888del , CM000667.1:g.1275880_1275888del	GRCh37
NC_000005.8:g.1328880_1328888del	NCBI36
NG_009265.1:g.24276_24284del , LRG_343:g.24276_24284del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2869_2286+2877del MANE Select	ENSP00000309572.5:n.2286+2869_2286+2877del
ENST00000656021.1:c.*1832+2869_*1832+2877del	ENSP00000499759.1:n.*1832+2869_*1832+2877del
ENST00000310581.9:c.2286+2869_2286+2877del	ENSP00000309572.5:n.2286+2869_2286+2877del
ENST00000334602.10:c.2286+2869_2286+2877del	ENSP00000334346.6:n.2286+2869_2286+2877del
ENST00000460137.6:c.2250+2869_2250+2877del	ENSP00000425003.1:n.2250+2869_2250+2877del
ENST00000484238.6:n.1099+2869_1099+2877del
ENST00000508104.2:c.2286+2869_2286+2877del	ENSP00000426042.2:n.2286+2869_2286+2877del
NM_001193376.1:c.2286+2869_2286+2877del	NP_001180305.1:n.2286+2869_2286+2877del
NM_198253.2:c.2286+2869_2286+2877del , LRG_343t1:c.2286+2869_2286+2877del	NP_937983.2:n.2286+2869_2286+2877del
XM_011514104.1:c.756+2869_756+2877del	XP_011512406.1:n.756+2869_756+2877del
XM_011514105.1:c.642+2869_642+2877del	XP_011512407.1:n.642+2869_642+2877del
XM_011514106.1:c.642+2869_642+2877del	XP_011512408.1:n.642+2869_642+2877del
NR_149162.1:n.2344+2869_2344+2877del
NR_149163.1:n.2308+2869_2308+2877del
NM_001193376.2:c.2286+2869_2286+2877del	NP_001180305.1:n.2286+2869_2286+2877del
NM_198253.3:c.2286+2869_2286+2877del MANE Select	NP_937983.2:n.2286+2869_2286+2877del
NR_149162.2:n.2365+2869_2365+2877del
NR_149163.2:n.2329+2869_2329+2877del
NM_001193376.3:c.2286+2869_2286+2877del	NP_001180305.1:n.2286+2869_2286+2877del
NR_149162.3:n.2365+2869_2365+2877del
NR_149163.3:n.2329+2869_2329+2877del