Canonical Allele Identifier: CA915943232

Gene: TERT

Linked Data

• ClinVar Variation Id: 654543
• ClinVar RCV Id: RCV002538074
• dbSNP Id: rs1579597416

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293993_1293994delinsTT , CM000667.2:g.1293993_1293994delinsTT	GRCh38
NC_000005.9:g.1294108_1294109delinsTT , CM000667.1:g.1294108_1294109delinsTT	GRCh37
NC_000005.8:g.1347108_1347109delinsTT	NCBI36
NG_009265.1:g.6054_6055delinsAA , LRG_343:g.6054_6055delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.892_893delinsAA MANE Select	ENSP00000309572.5:p.Ser298Asn
ENST00000656021.1:c.892_893delinsAA	ENSP00000499759.1:p.Ser298Asn
ENST00000310581.9:c.892_893delinsAA	ENSP00000309572.5:p.Ser298Asn
ENST00000334602.10:c.892_893delinsAA	ENSP00000334346.6:p.Ser298Asn
ENST00000460137.6:c.892_893delinsAA	ENSP00000425003.1:p.Ser298Asn
ENST00000508104.2:c.892_893delinsAA	ENSP00000426042.2:p.Ser298Asn
NM_001193376.1:c.892_893delinsAA	NP_001180305.1:p.Ser298Asn
NM_198253.2:c.892_893delinsAA , LRG_343t1:c.892_893delinsAA	NP_937983.2:p.Ser298Asn
NR_149162.1:n.950_951delinsAA
NR_149163.1:n.950_951delinsAA
NM_001193376.2:c.892_893delinsAA	NP_001180305.1:p.Ser298Asn
NM_198253.3:c.892_893delinsAA MANE Select	NP_937983.2:p.Ser298Asn
NR_149162.2:n.971_972delinsAA
NR_149163.2:n.971_972delinsAA
NM_001193376.3:c.892_893delinsAA	NP_001180305.1:p.Ser298Asn
NR_149162.3:n.971_972delinsAA
NR_149163.3:n.971_972delinsAA