Canonical Allele Identifier: CA1522565792

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1279453C= , CM000667.2:g.1279453C=	GRCh38
NC_000005.9:g.1279568C= , CM000667.1:g.1279568C=	GRCh37
NC_000005.8:g.1332568C=	NCBI36
NG_009265.1:g.20595G= , LRG_343:g.20595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1968G= MANE Select	ENSP00000309572.5:p.Ser656=
ENST00000656021.1:c.*1514G=	ENSP00000499759.1:n.*1514G=
ENST00000310581.9:c.1968G=	ENSP00000309572.5:p.Ser656=
ENST00000334602.10:c.1968G=	ENSP00000334346.6:p.Ser656=
ENST00000460137.6:c.1968G=	ENSP00000425003.1:p.Ser656=
ENST00000484238.6:n.781G=
ENST00000508104.2:c.1968G=	ENSP00000426042.2:p.Ser656=
NM_001193376.1:c.1968G=	NP_001180305.1:p.Ser656=
NM_198253.2:c.1968G= , LRG_343t1:c.1968G=	NP_937983.2:p.Ser656=
XM_011514104.1:c.438G=	XP_011512406.1:p.Ser146=
XM_011514105.1:c.324G=	XP_011512407.1:p.Ser108=
XM_011514106.1:c.324G=	XP_011512408.1:p.Ser108=
NR_149162.1:n.2026G=
NR_149163.1:n.2026G=
NM_001193376.2:c.1968G=	NP_001180305.1:p.Ser656=
NM_198253.3:c.1968G= MANE Select	NP_937983.2:p.Ser656=
NR_149162.2:n.2047G=
NR_149163.2:n.2047G=
NM_001193376.3:c.1968G=	NP_001180305.1:p.Ser656=
NR_149162.3:n.2047G=
NR_149163.3:n.2047G=