Canonical Allele Identifier: CA443239584

Gene: TERT

Linked Data

• ClinVar Variation Id: 1108397
• ClinVar RCV Id: RCV002439012 ; RCV002555183
• dbSNP Id: rs375423906
• gnomAD v4: 5-1294052-G-C
• MyVariant Identifiers: chr5:g.1294167G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294052G>C , CM000667.2:g.1294052G>C	GRCh38
NC_000005.9:g.1294167G>C , CM000667.1:g.1294167G>C	GRCh37
NC_000005.8:g.1347167G>C	NCBI36
NG_009265.1:g.5996C>G , LRG_343:g.5996C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.834C>G MANE Select	ENSP00000309572.5:p.Pro278=
ENST00000656021.1:c.834C>G	ENSP00000499759.1:p.Pro278=
ENST00000310581.9:c.834C>G	ENSP00000309572.5:p.Pro278=
ENST00000334602.10:c.834C>G	ENSP00000334346.6:p.Pro278=
ENST00000460137.6:c.834C>G	ENSP00000425003.1:p.Pro278=
ENST00000508104.2:c.834C>G	ENSP00000426042.2:p.Pro278=
NM_001193376.1:c.834C>G	NP_001180305.1:p.Pro278=
NM_198253.2:c.834C>G , LRG_343t1:c.834C>G	NP_937983.2:p.Pro278=
NR_149162.1:n.892C>G
NR_149163.1:n.892C>G
NM_001193376.2:c.834C>G	NP_001180305.1:p.Pro278=
NM_198253.3:c.834C>G MANE Select	NP_937983.2:p.Pro278=
NR_149162.2:n.913C>G
NR_149163.2:n.913C>G
NM_001193376.3:c.834C>G	NP_001180305.1:p.Pro278=
NR_149162.3:n.913C>G
NR_149163.3:n.913C>G