Canonical Allele Identifier: CA1522539510

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260235G= , CM000667.2:g.1260235G=	GRCh38
NC_000005.9:g.1260350G= , CM000667.1:g.1260350G=	GRCh37
NC_000005.8:g.1313350G=	NCBI36
NG_009265.1:g.39813C= , LRG_343:g.39813C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+239C= MANE Select	ENSP00000309572.5:n.2970+239C=
ENST00000656021.1:c.*2516+239C=	ENSP00000499759.1:n.*2516+239C=
ENST00000667927.1:n.258+239C=
ENST00000310581.9:c.2970+239C=	ENSP00000309572.5:n.2970+239C=
ENST00000334602.10:c.2781+239C=	ENSP00000334346.6:n.2781+239C=
ENST00000460137.6:c.2563+239C=	ENSP00000425003.1:n.2563+239C=
ENST00000484238.6:n.1412+239C=
NM_001193376.1:c.2781+239C=	NP_001180305.1:n.2781+239C=
NM_198253.2:c.2970+239C= , LRG_343t1:c.2970+239C=	NP_937983.2:n.2970+239C=
XM_011514104.1:c.1440+239C=	XP_011512406.1:n.1440+239C=
XM_011514105.1:c.1326+239C=	XP_011512407.1:n.1326+239C=
XM_011514106.1:c.1326+239C=	XP_011512408.1:n.1326+239C=
NR_149162.1:n.2657+239C=
NR_149163.1:n.2621+239C=
NM_001193376.2:c.2781+239C=	NP_001180305.1:n.2781+239C=
NM_198253.3:c.2970+239C= MANE Select	NP_937983.2:n.2970+239C=
NR_149162.2:n.2678+239C=
NR_149163.2:n.2642+239C=
NM_001193376.3:c.2781+239C=	NP_001180305.1:n.2781+239C=
NR_149162.3:n.2678+239C=
NR_149163.3:n.2642+239C=