Canonical Allele Identifier: CA443005882

Gene: TERT

Linked Data

• ClinVar Variation Id: 1673336
• ClinVar RCV Id: RCV003089092
• dbSNP Id: rs1751295827
• gnomAD v4: 5-1294879-C-T
• MyVariant Identifiers: chr5:g.1294994C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294879C>T , CM000667.2:g.1294879C>T	GRCh38
NC_000005.9:g.1294994C>T , CM000667.1:g.1294994C>T	GRCh37
NC_000005.8:g.1347994C>T	NCBI36
NG_009265.1:g.5169G>A , LRG_343:g.5169G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.111G>A MANE Select	ENSP00000309572.5:p.Arg37=
ENST00000656021.1:c.111G>A	ENSP00000499759.1:p.Arg37=
ENST00000310581.9:c.111G>A	ENSP00000309572.5:p.Arg37=
ENST00000334602.10:c.111G>A	ENSP00000334346.6:p.Arg37=
ENST00000460137.6:c.111G>A	ENSP00000425003.1:p.Arg37=
ENST00000508104.2:c.111G>A	ENSP00000426042.2:p.Arg37=
ENST00000522877.1:n.191G>A
NM_001193376.1:c.111G>A	NP_001180305.1:p.Arg37=
NM_198253.2:c.111G>A , LRG_343t1:c.111G>A	NP_937983.2:p.Arg37=
NR_149162.1:n.169G>A
NR_149163.1:n.169G>A
NM_001193376.2:c.111G>A	NP_001180305.1:p.Arg37=
NM_198253.3:c.111G>A MANE Select	NP_937983.2:p.Arg37=
NR_149162.2:n.190G>A
NR_149163.2:n.190G>A
NM_001193376.3:c.111G>A	NP_001180305.1:p.Arg37=
NR_149162.3:n.190G>A
NR_149163.3:n.190G>A