Canonical Allele Identifier: CA359080756

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1279543G>A (hg19) ; chr5:g.1279428G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1279428G>A , CM000667.2:g.1279428G>A	GRCh38
NC_000005.9:g.1279543G>A , CM000667.1:g.1279543G>A	GRCh37
NC_000005.8:g.1332543G>A	NCBI36
NG_009265.1:g.20620C>T , LRG_343:g.20620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1993C>T MANE Select	ENSP00000309572.5:p.Leu665Phe
ENST00000656021.1:c.*1539C>T	ENSP00000499759.1:n.*1539C>T
ENST00000310581.9:c.1993C>T	ENSP00000309572.5:p.Leu665Phe
ENST00000334602.10:c.1993C>T	ENSP00000334346.6:p.Leu665Phe
ENST00000460137.6:c.1993C>T	ENSP00000425003.1:p.Leu665Phe
ENST00000484238.6:n.806C>T
ENST00000508104.2:c.1993C>T	ENSP00000426042.2:p.Leu665Phe
NM_001193376.1:c.1993C>T	NP_001180305.1:p.Leu665Phe
NM_198253.2:c.1993C>T , LRG_343t1:c.1993C>T	NP_937983.2:p.Leu665Phe
XM_011514104.1:c.463C>T	XP_011512406.1:p.Leu155Phe
XM_011514105.1:c.349C>T	XP_011512407.1:p.Leu117Phe
XM_011514106.1:c.349C>T	XP_011512408.1:p.Leu117Phe
NR_149162.1:n.2051C>T
NR_149163.1:n.2051C>T
NM_001193376.2:c.1993C>T	NP_001180305.1:p.Leu665Phe
NM_198253.3:c.1993C>T MANE Select	NP_937983.2:p.Leu665Phe
NR_149162.2:n.2072C>T
NR_149163.2:n.2072C>T
NM_001193376.3:c.1993C>T	NP_001180305.1:p.Leu665Phe
NR_149162.3:n.2072C>T
NR_149163.3:n.2072C>T