Canonical Allele Identifier: CA359056584
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1524765
ClinVar RCV Id: RCV002550494
dbSNP Id: rs2126687588
gnomAD v4: 5-1294054-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1294054G>A , CM000667.2:g.1294054G>A GRCh38
NC_000005.9:g.1294169G>A , CM000667.1:g.1294169G>A GRCh37
NC_000005.8:g.1347169G>A NCBI36
NG_009265.1:g.5994C>T , LRG_343:g.5994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.832C>T MANE Select ENSP00000309572.5:p.Pro278Ser
ENST00000656021.1:c.832C>T ENSP00000499759.1:p.Pro278Ser
ENST00000310581.9:c.832C>T ENSP00000309572.5:p.Pro278Ser
ENST00000334602.10:c.832C>T ENSP00000334346.6:p.Pro278Ser
ENST00000460137.6:c.832C>T ENSP00000425003.1:p.Pro278Ser
ENST00000508104.2:c.832C>T ENSP00000426042.2:p.Pro278Ser
NM_001193376.1:c.832C>T NP_001180305.1:p.Pro278Ser
NM_198253.2:c.832C>T , LRG_343t1:c.832C>T NP_937983.2:p.Pro278Ser
NR_149162.1:n.890C>T
NR_149163.1:n.890C>T
NM_001193376.2:c.832C>T NP_001180305.1:p.Pro278Ser
NM_198253.3:c.832C>T MANE Select NP_937983.2:p.Pro278Ser
NR_149162.2:n.911C>T
NR_149163.2:n.911C>T
NM_001193376.3:c.832C>T NP_001180305.1:p.Pro278Ser
NR_149162.3:n.911C>T
NR_149163.3:n.911C>T