Canonical Allele Identifier: CA645540791

Gene: TERT

Linked Data

• COSMIC: COSM4385839

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294961_1294984del , CM000667.2:g.1294961_1294984del	GRCh38
NC_000005.9:g.1295076_1295099del , CM000667.1:g.1295076_1295099del	GRCh37
NC_000005.8:g.1348076_1348099del	NCBI36
NG_009265.1:g.5068_5091del , LRG_343:g.5068_5091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.10_33del MANE Select	ENSP00000309572.5:p.Ala4_Arg11del
ENST00000656021.1:c.10_33del	ENSP00000499759.1:p.Ala4_Arg11del
ENST00000310581.9:c.10_33del	ENSP00000309572.5:p.Ala4_Arg11del
ENST00000334602.10:c.10_33del	ENSP00000334346.6:p.Ala4_Arg11del
ENST00000460137.6:c.10_33del	ENSP00000425003.1:p.Ala4_Arg11del
ENST00000508104.2:c.10_33del	ENSP00000426042.2:p.Ala4_Arg11del
ENST00000522877.1:n.90_113del
NM_001193376.1:c.10_33del	NP_001180305.1:p.Ala4_Arg11del
NM_198253.2:c.10_33del , LRG_343t1:c.10_33del	NP_937983.2:p.Ala4_Arg11del
NR_149162.1:n.68_91del
NR_149163.1:n.68_91del
NM_001193376.2:c.10_33del	NP_001180305.1:p.Ala4_Arg11del
NM_198253.3:c.10_33del MANE Select	NP_937983.2:p.Ala4_Arg11del
NR_149162.2:n.89_112del
NR_149163.2:n.89_112del
NM_001193376.3:c.10_33del	NP_001180305.1:p.Ala4_Arg11del
NR_149162.3:n.89_112del
NR_149163.3:n.89_112del