Canonical Allele Identifier: CA359078672

Gene: TERT

Linked Data

• ClinVar Variation Id: 972247
• ClinVar RCV Id: RCV002447228 ; RCV002570372
• dbSNP Id: rs1749780917
• gnomAD v4: 5-1278645-C-T
• MyVariant Identifiers: chr5:g.1278760C>T (hg19) ; chr5:g.1278645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278645C>T , CM000667.2:g.1278645C>T	GRCh38
NC_000005.9:g.1278760C>T , CM000667.1:g.1278760C>T	GRCh37
NC_000005.8:g.1331760C>T	NCBI36
NG_009265.1:g.21403G>A , LRG_343:g.21403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2282G>A MANE Select	ENSP00000309572.5:p.Ser761Asn
ENST00000656021.1:c.*1828G>A	ENSP00000499759.1:n.*1828G>A
ENST00000310581.9:c.2282G>A	ENSP00000309572.5:p.Ser761Asn
ENST00000334602.10:c.2282G>A	ENSP00000334346.6:p.Ser761Asn
ENST00000460137.6:c.2246G>A	ENSP00000425003.1:p.Ser749Asn
ENST00000484238.6:n.1095G>A
ENST00000508104.2:c.2282G>A	ENSP00000426042.2:p.Ser761Asn
NM_001193376.1:c.2282G>A	NP_001180305.1:p.Ser761Asn
NM_198253.2:c.2282G>A , LRG_343t1:c.2282G>A	NP_937983.2:p.Ser761Asn
XM_011514104.1:c.752G>A	XP_011512406.1:p.Ser251Asn
XM_011514105.1:c.638G>A	XP_011512407.1:p.Ser213Asn
XM_011514106.1:c.638G>A	XP_011512408.1:p.Ser213Asn
NR_149162.1:n.2340G>A
NR_149163.1:n.2304G>A
NM_001193376.2:c.2282G>A	NP_001180305.1:p.Ser761Asn
NM_198253.3:c.2282G>A MANE Select	NP_937983.2:p.Ser761Asn
NR_149162.2:n.2361G>A
NR_149163.2:n.2325G>A
NM_001193376.3:c.2282G>A	NP_001180305.1:p.Ser761Asn
NR_149162.3:n.2361G>A
NR_149163.3:n.2325G>A