Canonical Allele Identifier: CA443024477

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278807G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278692G>T , CM000667.2:g.1278692G>T	GRCh38
NC_000005.9:g.1278807G>T , CM000667.1:g.1278807G>T	GRCh37
NC_000005.8:g.1331807G>T	NCBI36
NG_009265.1:g.21356C>A , LRG_343:g.21356C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2235C>A MANE Select	ENSP00000309572.5:p.Ala745=
ENST00000656021.1:c.*1781C>A	ENSP00000499759.1:n.*1781C>A
ENST00000310581.9:c.2235C>A	ENSP00000309572.5:p.Ala745=
ENST00000334602.10:c.2235C>A	ENSP00000334346.6:p.Ala745=
ENST00000460137.6:c.2199C>A	ENSP00000425003.1:p.Ala733=
ENST00000484238.6:n.1048C>A
ENST00000508104.2:c.2235C>A	ENSP00000426042.2:p.Ala745=
NM_001193376.1:c.2235C>A	NP_001180305.1:p.Ala745=
NM_198253.2:c.2235C>A , LRG_343t1:c.2235C>A	NP_937983.2:p.Ala745=
XM_011514104.1:c.705C>A	XP_011512406.1:p.Ala235=
XM_011514105.1:c.591C>A	XP_011512407.1:p.Ala197=
XM_011514106.1:c.591C>A	XP_011512408.1:p.Ala197=
NR_149162.1:n.2293C>A
NR_149163.1:n.2257C>A
NM_001193376.2:c.2235C>A	NP_001180305.1:p.Ala745=
NM_198253.3:c.2235C>A MANE Select	NP_937983.2:p.Ala745=
NR_149162.2:n.2314C>A
NR_149163.2:n.2278C>A
NM_001193376.3:c.2235C>A	NP_001180305.1:p.Ala745=
NR_149162.3:n.2314C>A
NR_149163.3:n.2278C>A