Canonical Allele Identifier: CA1522555448

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293622C= , CM000667.2:g.1293622C=	GRCh38
NC_000005.9:g.1293737C= , CM000667.1:g.1293737C=	GRCh37
NC_000005.8:g.1346737C=	NCBI36
NG_009265.1:g.6426G= , LRG_343:g.6426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1264G= MANE Select	ENSP00000309572.5:p.Ala422=
ENST00000656021.1:c.1264G=	ENSP00000499759.1:p.Ala422=
ENST00000310581.9:c.1264G=	ENSP00000309572.5:p.Ala422=
ENST00000334602.10:c.1264G=	ENSP00000334346.6:p.Ala422=
ENST00000460137.6:c.1264G=	ENSP00000425003.1:p.Ala422=
ENST00000508104.2:c.1264G=	ENSP00000426042.2:p.Ala422=
NM_001193376.1:c.1264G=	NP_001180305.1:p.Ala422=
NM_198253.2:c.1264G= , LRG_343t1:c.1264G=	NP_937983.2:p.Ala422=
NR_149162.1:n.1322G=
NR_149163.1:n.1322G=
NM_001193376.2:c.1264G=	NP_001180305.1:p.Ala422=
NM_198253.3:c.1264G= MANE Select	NP_937983.2:p.Ala422=
NR_149162.2:n.1343G=
NR_149163.2:n.1343G=
NM_001193376.3:c.1264G=	NP_001180305.1:p.Ala422=
NR_149162.3:n.1343G=
NR_149163.3:n.1343G=