Canonical Allele Identifier: CA443240684

Gene: TERT

Linked Data

• ClinVar Variation Id: 700225
• ClinVar RCV Id: RCV002332804 ; RCV002536787
• dbSNP Id: rs1233765307
• gnomAD v2: 5-1293825-C-G
• gnomAD v3: 5-1293710-C-G
• gnomAD v4: 5-1293710-C-G
• MyVariant Identifiers: chr5:g.1293825C>G (hg19) ; chr5:g.1293710C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293710C>G , CM000667.2:g.1293710C>G	GRCh38
NC_000005.9:g.1293825C>G , CM000667.1:g.1293825C>G	GRCh37
NC_000005.8:g.1346825C>G	NCBI36
NG_009265.1:g.6338G>C , LRG_343:g.6338G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1176G>C MANE Select	ENSP00000309572.5:p.Leu392=
ENST00000656021.1:c.1176G>C	ENSP00000499759.1:p.Leu392=
ENST00000310581.9:c.1176G>C	ENSP00000309572.5:p.Leu392=
ENST00000334602.10:c.1176G>C	ENSP00000334346.6:p.Leu392=
ENST00000460137.6:c.1176G>C	ENSP00000425003.1:p.Leu392=
ENST00000508104.2:c.1176G>C	ENSP00000426042.2:p.Leu392=
NM_001193376.1:c.1176G>C	NP_001180305.1:p.Leu392=
NM_198253.2:c.1176G>C , LRG_343t1:c.1176G>C	NP_937983.2:p.Leu392=
NR_149162.1:n.1234G>C
NR_149163.1:n.1234G>C
NM_001193376.2:c.1176G>C	NP_001180305.1:p.Leu392=
NM_198253.3:c.1176G>C MANE Select	NP_937983.2:p.Leu392=
NR_149162.2:n.1255G>C
NR_149163.2:n.1255G>C
NM_001193376.3:c.1176G>C	NP_001180305.1:p.Leu392=
NR_149162.3:n.1255G>C
NR_149163.3:n.1255G>C