Canonical Allele Identifier: CA443024291

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278768G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278653G>C , CM000667.2:g.1278653G>C	GRCh38
NC_000005.9:g.1278768G>C , CM000667.1:g.1278768G>C	GRCh37
NC_000005.8:g.1331768G>C	NCBI36
NG_009265.1:g.21395C>G , LRG_343:g.21395C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2274C>G MANE Select	ENSP00000309572.5:p.Ala758=
ENST00000656021.1:c.*1820C>G	ENSP00000499759.1:n.*1820C>G
ENST00000310581.9:c.2274C>G	ENSP00000309572.5:p.Ala758=
ENST00000334602.10:c.2274C>G	ENSP00000334346.6:p.Ala758=
ENST00000460137.6:c.2238C>G	ENSP00000425003.1:p.Ala746=
ENST00000484238.6:n.1087C>G
ENST00000508104.2:c.2274C>G	ENSP00000426042.2:p.Ala758=
NM_001193376.1:c.2274C>G	NP_001180305.1:p.Ala758=
NM_198253.2:c.2274C>G , LRG_343t1:c.2274C>G	NP_937983.2:p.Ala758=
XM_011514104.1:c.744C>G	XP_011512406.1:p.Ala248=
XM_011514105.1:c.630C>G	XP_011512407.1:p.Ala210=
XM_011514106.1:c.630C>G	XP_011512408.1:p.Ala210=
NR_149162.1:n.2332C>G
NR_149163.1:n.2296C>G
NM_001193376.2:c.2274C>G	NP_001180305.1:p.Ala758=
NM_198253.3:c.2274C>G MANE Select	NP_937983.2:p.Ala758=
NR_149162.2:n.2353C>G
NR_149163.2:n.2317C>G
NM_001193376.3:c.2274C>G	NP_001180305.1:p.Ala758=
NR_149162.3:n.2353C>G
NR_149163.3:n.2317C>G