Canonical Allele Identifier: CA1522558859

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294745C= , CM000667.2:g.1294745C=	GRCh38
NC_000005.9:g.1294860C= , CM000667.1:g.1294860C=	GRCh37
NC_000005.8:g.1347860C=	NCBI36
NG_009265.1:g.5303G= , LRG_343:g.5303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.219+26G= MANE Select	ENSP00000309572.5:n.219+26G=
ENST00000656021.1:c.219+26G=	ENSP00000499759.1:n.219+26G=
ENST00000310581.9:c.219+26G=	ENSP00000309572.5:n.219+26G=
ENST00000334602.10:c.219+26G=	ENSP00000334346.6:n.219+26G=
ENST00000460137.6:c.219+26G=	ENSP00000425003.1:n.219+26G=
ENST00000508104.2:c.219+26G=	ENSP00000426042.2:n.219+26G=
ENST00000522877.1:n.299+26G=
NM_001193376.1:c.219+26G=	NP_001180305.1:n.219+26G=
NM_198253.2:c.219+26G= , LRG_343t1:c.219+26G=	NP_937983.2:n.219+26G=
NR_149162.1:n.277+26G=
NR_149163.1:n.277+26G=
NM_001193376.2:c.219+26G=	NP_001180305.1:n.219+26G=
NM_198253.3:c.219+26G= MANE Select	NP_937983.2:n.219+26G=
NR_149162.2:n.298+26G=
NR_149163.2:n.298+26G=
NM_001193376.3:c.219+26G=	NP_001180305.1:n.219+26G=
NR_149162.3:n.298+26G=
NR_149163.3:n.298+26G=