Canonical Allele Identifier: CA1522539729

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260432C= , CM000667.2:g.1260432C=	GRCh38
NC_000005.9:g.1260547C= , CM000667.1:g.1260547C=	GRCh37
NC_000005.8:g.1313547C=	NCBI36
NG_009265.1:g.39616G= , LRG_343:g.39616G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+42G= MANE Select	ENSP00000309572.5:n.2970+42G=
ENST00000656021.1:c.*2516+42G=	ENSP00000499759.1:n.*2516+42G=
ENST00000667927.1:n.258+42G=
ENST00000310581.9:c.2970+42G=	ENSP00000309572.5:n.2970+42G=
ENST00000334602.10:c.2781+42G=	ENSP00000334346.6:n.2781+42G=
ENST00000460137.6:c.2563+42G=	ENSP00000425003.1:n.2563+42G=
ENST00000484238.6:n.1412+42G=
NM_001193376.1:c.2781+42G=	NP_001180305.1:n.2781+42G=
NM_198253.2:c.2970+42G= , LRG_343t1:c.2970+42G=	NP_937983.2:n.2970+42G=
XM_011514104.1:c.1440+42G=	XP_011512406.1:n.1440+42G=
XM_011514105.1:c.1326+42G=	XP_011512407.1:n.1326+42G=
XM_011514106.1:c.1326+42G=	XP_011512408.1:n.1326+42G=
NR_149162.1:n.2657+42G=
NR_149163.1:n.2621+42G=
NM_001193376.2:c.2781+42G=	NP_001180305.1:n.2781+42G=
NM_198253.3:c.2970+42G= MANE Select	NP_937983.2:n.2970+42G=
NR_149162.2:n.2678+42G=
NR_149163.2:n.2642+42G=
NM_001193376.3:c.2781+42G=	NP_001180305.1:n.2781+42G=
NR_149162.3:n.2678+42G=
NR_149163.3:n.2642+42G=