Canonical Allele Identifier: CA359085170

Gene: TERT

Linked Data

• ClinVar Variation Id: 539185
• ClinVar RCV Id: RCV002388122 ; RCV002533362
• dbSNP Id: rs1554042799
• MyVariant Identifiers: chr5:g.1293475G>A (hg19) ; chr5:g.1293360G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293360G>A , CM000667.2:g.1293360G>A	GRCh38
NC_000005.9:g.1293475G>A , CM000667.1:g.1293475G>A	GRCh37
NC_000005.8:g.1346475G>A	NCBI36
NG_009265.1:g.6688C>T , LRG_343:g.6688C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1526C>T MANE Select	ENSP00000309572.5:p.Thr509Met
ENST00000656021.1:c.1526C>T	ENSP00000499759.1:p.Thr509Met
ENST00000310581.9:c.1526C>T	ENSP00000309572.5:p.Thr509Met
ENST00000334602.10:c.1526C>T	ENSP00000334346.6:p.Thr509Met
ENST00000460137.6:c.1526C>T	ENSP00000425003.1:p.Thr509Met
ENST00000508104.2:c.1526C>T	ENSP00000426042.2:p.Thr509Met
NM_001193376.1:c.1526C>T	NP_001180305.1:p.Thr509Met
NM_198253.2:c.1526C>T , LRG_343t1:c.1526C>T	NP_937983.2:p.Thr509Met
NR_149162.1:n.1584C>T
NR_149163.1:n.1584C>T
NM_001193376.2:c.1526C>T	NP_001180305.1:p.Thr509Met
NM_198253.3:c.1526C>T MANE Select	NP_937983.2:p.Thr509Met
NR_149162.2:n.1605C>T
NR_149163.2:n.1605C>T
NM_001193376.3:c.1526C>T	NP_001180305.1:p.Thr509Met
NR_149162.3:n.1605C>T
NR_149163.3:n.1605C>T