Canonical Allele Identifier: CA803617202

Gene: TERT

Linked Data

• dbSNP Id: rs1248098613
• MyVariant Identifiers: chr5:g.1286620del (hg19) ; chr5:g.1286505del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1286510del , CM000667.2:g.1286510del	GRCh38
NC_000005.9:g.1286625del , CM000667.1:g.1286625del	GRCh37
NC_000005.8:g.1339625del	NCBI36
NG_009265.1:g.13543del , LRG_343:g.13543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1574-3881del MANE Select	ENSP00000309572.5:n.1574-3881del
ENST00000656021.1:c.*779del	ENSP00000499759.1:n.*779del
ENST00000310581.9:c.1574-3881del	ENSP00000309572.5:n.1574-3881del
ENST00000334602.10:c.1574-3881del	ENSP00000334346.6:n.1574-3881del
ENST00000460137.6:c.1574-3881del	ENSP00000425003.1:n.1574-3881del
ENST00000508104.2:c.1574-3881del	ENSP00000426042.2:n.1574-3881del
NM_001193376.1:c.1574-3881del	NP_001180305.1:n.1574-3881del
NM_198253.2:c.1574-3881del , LRG_343t1:c.1574-3881del	NP_937983.2:n.1574-3881del
XM_011514104.1:c.-298del	XP_011512406.1:n.-298del
XM_011514105.1:c.-453del	XP_011512407.1:n.-453del
NR_149162.1:n.1632-3881del
NR_149163.1:n.1632-3881del
NM_001193376.2:c.1574-3881del	NP_001180305.1:n.1574-3881del
NM_198253.3:c.1574-3881del MANE Select	NP_937983.2:n.1574-3881del
NR_149162.2:n.1653-3881del
NR_149163.2:n.1653-3881del
NM_001193376.3:c.1574-3881del	NP_001180305.1:n.1574-3881del
NR_149162.3:n.1653-3881del
NR_149163.3:n.1653-3881del