Canonical Allele Identifier: CA443024877

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1279514G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1279399G>C , CM000667.2:g.1279399G>C	GRCh38
NC_000005.9:g.1279514G>C , CM000667.1:g.1279514G>C	GRCh37
NC_000005.8:g.1332514G>C	NCBI36
NG_009265.1:g.20649C>G , LRG_343:g.20649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2022C>G MANE Select	ENSP00000309572.5:p.Gly674=
ENST00000656021.1:c.*1568C>G	ENSP00000499759.1:n.*1568C>G
ENST00000310581.9:c.2022C>G	ENSP00000309572.5:p.Gly674=
ENST00000334602.10:c.2022C>G	ENSP00000334346.6:p.Gly674=
ENST00000460137.6:c.2022C>G	ENSP00000425003.1:p.Gly674=
ENST00000484238.6:n.835C>G
ENST00000508104.2:c.2022C>G	ENSP00000426042.2:p.Gly674=
NM_001193376.1:c.2022C>G	NP_001180305.1:p.Gly674=
NM_198253.2:c.2022C>G , LRG_343t1:c.2022C>G	NP_937983.2:p.Gly674=
XM_011514104.1:c.492C>G	XP_011512406.1:p.Gly164=
XM_011514105.1:c.378C>G	XP_011512407.1:p.Gly126=
XM_011514106.1:c.378C>G	XP_011512408.1:p.Gly126=
NR_149162.1:n.2080C>G
NR_149163.1:n.2080C>G
NM_001193376.2:c.2022C>G	NP_001180305.1:p.Gly674=
NM_198253.3:c.2022C>G MANE Select	NP_937983.2:p.Gly674=
NR_149162.2:n.2101C>G
NR_149163.2:n.2101C>G
NM_001193376.3:c.2022C>G	NP_001180305.1:p.Gly674=
NR_149162.3:n.2101C>G
NR_149163.3:n.2101C>G