Canonical Allele Identifier: CA443021938

Gene: TERT

Linked Data

• gnomAD v4: 5-1266502-C-T
• MyVariant Identifiers: chr5:g.1266617C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266502C>T , CM000667.2:g.1266502C>T	GRCh38
NC_000005.9:g.1266617C>T , CM000667.1:g.1266617C>T	GRCh37
NC_000005.8:g.1319617C>T	NCBI36
NG_009265.1:g.33546G>A , LRG_343:g.33546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2616G>A MANE Select	ENSP00000309572.5:p.Leu872=
ENST00000656021.1:c.*2162G>A	ENSP00000499759.1:n.*2162G>A
ENST00000310581.9:c.2616G>A	ENSP00000309572.5:p.Leu872=
ENST00000334602.10:c.2616G>A	ENSP00000334346.6:p.Leu872=
ENST00000460137.6:c.2398G>A	ENSP00000425003.1:n.2398G>A
ENST00000484238.6:n.1247G>A
ENST00000503656.1:n.23G>A
ENST00000508104.2:c.2434G>A	ENSP00000426042.2:n.2434G>A
NM_001193376.1:c.2616G>A	NP_001180305.1:p.Leu872=
NM_198253.2:c.2616G>A , LRG_343t1:c.2616G>A	NP_937983.2:p.Leu872=
XM_011514104.1:c.1086G>A	XP_011512406.1:p.Leu362=
XM_011514105.1:c.972G>A	XP_011512407.1:p.Leu324=
XM_011514106.1:c.972G>A	XP_011512408.1:p.Leu324=
NR_149162.1:n.2492G>A
NR_149163.1:n.2456G>A
NM_001193376.2:c.2616G>A	NP_001180305.1:p.Leu872=
NM_198253.3:c.2616G>A MANE Select	NP_937983.2:p.Leu872=
NR_149162.2:n.2513G>A
NR_149163.2:n.2477G>A
NM_001193376.3:c.2616G>A	NP_001180305.1:p.Leu872=
NR_149162.3:n.2513G>A
NR_149163.3:n.2477G>A