Canonical Allele Identifier: CA359078775

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278769G>T (hg19) ; chr5:g.1278654G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278654G>T , CM000667.2:g.1278654G>T	GRCh38
NC_000005.9:g.1278769G>T , CM000667.1:g.1278769G>T	GRCh37
NC_000005.8:g.1331769G>T	NCBI36
NG_009265.1:g.21394C>A , LRG_343:g.21394C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2273C>A MANE Select	ENSP00000309572.5:p.Ala758Asp
ENST00000656021.1:c.*1819C>A	ENSP00000499759.1:n.*1819C>A
ENST00000310581.9:c.2273C>A	ENSP00000309572.5:p.Ala758Asp
ENST00000334602.10:c.2273C>A	ENSP00000334346.6:p.Ala758Asp
ENST00000460137.6:c.2237C>A	ENSP00000425003.1:p.Ala746Asp
ENST00000484238.6:n.1086C>A
ENST00000508104.2:c.2273C>A	ENSP00000426042.2:p.Ala758Asp
NM_001193376.1:c.2273C>A	NP_001180305.1:p.Ala758Asp
NM_198253.2:c.2273C>A , LRG_343t1:c.2273C>A	NP_937983.2:p.Ala758Asp
XM_011514104.1:c.743C>A	XP_011512406.1:p.Ala248Asp
XM_011514105.1:c.629C>A	XP_011512407.1:p.Ala210Asp
XM_011514106.1:c.629C>A	XP_011512408.1:p.Ala210Asp
NR_149162.1:n.2331C>A
NR_149163.1:n.2295C>A
NM_001193376.2:c.2273C>A	NP_001180305.1:p.Ala758Asp
NM_198253.3:c.2273C>A MANE Select	NP_937983.2:p.Ala758Asp
NR_149162.2:n.2352C>A
NR_149163.2:n.2316C>A
NM_001193376.3:c.2273C>A	NP_001180305.1:p.Ala758Asp
NR_149162.3:n.2352C>A
NR_149163.3:n.2316C>A