Canonical Allele Identifier: CA2673077934

Gene: TERT

Linked Data

• gnomAD v4: 5-1266652-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266652A>G , CM000667.2:g.1266652A>G	GRCh38
NC_000005.9:g.1266767A>G , CM000667.1:g.1266767A>G	GRCh37
NC_000005.8:g.1319767A>G	NCBI36
NG_009265.1:g.33396T>C , LRG_343:g.33396T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2583-117T>C MANE Select	ENSP00000309572.5:n.2583-117T>C
ENST00000656021.1:c.*2129-117T>C	ENSP00000499759.1:n.*2129-117T>C
ENST00000310581.9:c.2583-117T>C	ENSP00000309572.5:n.2583-117T>C
ENST00000334602.10:c.2583-117T>C	ENSP00000334346.6:n.2583-117T>C
ENST00000460137.6:c.2365-117T>C	ENSP00000425003.1:n.2365-117T>C
ENST00000484238.6:n.1214-117T>C
ENST00000508104.2:c.2401-117T>C	ENSP00000426042.2:n.2401-117T>C
NM_001193376.1:c.2583-117T>C	NP_001180305.1:n.2583-117T>C
NM_198253.2:c.2583-117T>C , LRG_343t1:c.2583-117T>C	NP_937983.2:n.2583-117T>C
XM_011514104.1:c.1053-117T>C	XP_011512406.1:n.1053-117T>C
XM_011514105.1:c.939-117T>C	XP_011512407.1:n.939-117T>C
XM_011514106.1:c.939-117T>C	XP_011512408.1:n.939-117T>C
NR_149162.1:n.2459-117T>C
NR_149163.1:n.2423-117T>C
NM_001193376.2:c.2583-117T>C	NP_001180305.1:n.2583-117T>C
NM_198253.3:c.2583-117T>C MANE Select	NP_937983.2:n.2583-117T>C
NR_149162.2:n.2480-117T>C
NR_149163.2:n.2444-117T>C
NM_001193376.3:c.2583-117T>C	NP_001180305.1:n.2583-117T>C
NR_149162.3:n.2480-117T>C
NR_149163.3:n.2444-117T>C