Canonical Allele Identifier: CA1522559385

Gene: TERT

Linked Data

• ClinVar Variation Id: 1041593
• ClinVar RCV Id: RCV002547032
• dbSNP Id: rs1751310344

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1295046del , CM000667.2:g.1295046del	GRCh38
NC_000005.9:g.1295161del , CM000667.1:g.1295161del	GRCh37
NC_000005.8:g.1348161del	NCBI36
NG_009265.1:g.5002del , LRG_343:g.5002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.-57del MANE Select	ENSP00000309572.5:n.-57del
ENST00000656021.1:c.-57del	ENSP00000499759.1:n.-57del
ENST00000310581.9:c.-57del	ENSP00000309572.5:n.-57del
ENST00000522877.1:n.24del
NM_001193376.1:c.-57del	NP_001180305.1:n.-57del
NM_198253.2:c.-57del , LRG_343t1:c.-57del	NP_937983.2:n.-57del
NR_149162.1:n.2del
NR_149163.1:n.2del
NM_001193376.2:c.-57del	NP_001180305.1:n.-57del
NM_198253.3:c.-57del MANE Select	NP_937983.2:n.-57del
NR_149162.2:n.23del
NR_149163.2:n.23del
NM_001193376.3:c.-57del	NP_001180305.1:n.-57del
NR_149162.3:n.23del
NR_149163.3:n.23del