Canonical Allele Identifier: CA443240676

Gene: TERT

Linked Data

• ClinVar Variation Id: 793982
• ClinVar RCV Id: RCV001441799
• dbSNP Id: rs1579596372
• gnomAD v4: 5-1293461-T-G
• MyVariant Identifiers: chr5:g.1293576T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293461T>G , CM000667.2:g.1293461T>G	GRCh38
NC_000005.9:g.1293576T>G , CM000667.1:g.1293576T>G	GRCh37
NC_000005.8:g.1346576T>G	NCBI36
NG_009265.1:g.6587A>C , LRG_343:g.6587A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.1425A>C MANE Select	ENSP00000309572.5:p.Pro475=
ENST00000656021.1:c.1425A>C	ENSP00000499759.1:p.Pro475=
ENST00000310581.9:c.1425A>C	ENSP00000309572.5:p.Pro475=
ENST00000334602.10:c.1425A>C	ENSP00000334346.6:p.Pro475=
ENST00000460137.6:c.1425A>C	ENSP00000425003.1:p.Pro475=
ENST00000508104.2:c.1425A>C	ENSP00000426042.2:p.Pro475=
NM_001193376.1:c.1425A>C	NP_001180305.1:p.Pro475=
NM_198253.2:c.1425A>C , LRG_343t1:c.1425A>C	NP_937983.2:p.Pro475=
NR_149162.1:n.1483A>C
NR_149163.1:n.1483A>C
NM_001193376.2:c.1425A>C	NP_001180305.1:p.Pro475=
NM_198253.3:c.1425A>C MANE Select	NP_937983.2:p.Pro475=
NR_149162.2:n.1504A>C
NR_149163.2:n.1504A>C
NM_001193376.3:c.1425A>C	NP_001180305.1:p.Pro475=
NR_149162.3:n.1504A>C
NR_149163.3:n.1504A>C