Canonical Allele Identifier: CA1522574214

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1285964G= , CM000667.2:g.1285964G=	GRCh38
NC_000005.9:g.1286079G= , CM000667.1:g.1286079G=	GRCh37
NC_000005.8:g.1339079G=	NCBI36
NG_009265.1:g.14084C= , LRG_343:g.14084C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.1574-3340C= MANE Select	ENSP00000309572.5:n.1574-3340C=
ENST00000656021.1:c.*1119+201C=	ENSP00000499759.1:n.*1119+201C=
ENST00000310581.9:c.1574-3340C=	ENSP00000309572.5:n.1574-3340C=
ENST00000334602.10:c.1574-3340C=	ENSP00000334346.6:n.1574-3340C=
ENST00000460137.6:c.1574-3340C=	ENSP00000425003.1:n.1574-3340C=
ENST00000508104.2:c.1574-3340C=	ENSP00000426042.2:n.1574-3340C=
NM_001193376.1:c.1574-3340C=	NP_001180305.1:n.1574-3340C=
NM_198253.2:c.1574-3340C= , LRG_343t1:c.1574-3340C=	NP_937983.2:n.1574-3340C=
XM_011514104.1:c.43+201C=	XP_011512406.1:n.43+201C=
XM_011514105.1:c.-72+160C=	XP_011512407.1:n.-72+160C=
XM_011514106.1:c.-137C=	XP_011512408.1:n.-137C=
NR_149162.1:n.1632-3340C=
NR_149163.1:n.1632-3340C=
NM_001193376.2:c.1574-3340C=	NP_001180305.1:n.1574-3340C=
NM_198253.3:c.1574-3340C= MANE Select	NP_937983.2:n.1574-3340C=
NR_149162.2:n.1653-3340C=
NR_149163.2:n.1653-3340C=
NM_001193376.3:c.1574-3340C=	NP_001180305.1:n.1574-3340C=
NR_149162.3:n.1653-3340C=
NR_149163.3:n.1653-3340C=