Canonical Allele Identifier: CA1522539340

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260046G= , CM000667.2:g.1260046G=	GRCh38
NC_000005.9:g.1260161G= , CM000667.1:g.1260161G=	GRCh37
NC_000005.8:g.1313161G=	NCBI36
NG_009265.1:g.40002C= , LRG_343:g.40002C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+428C= MANE Select	ENSP00000309572.5:n.2970+428C=
ENST00000656021.1:c.*2516+428C=	ENSP00000499759.1:n.*2516+428C=
ENST00000667927.1:n.258+428C=
ENST00000310581.9:c.2970+428C=	ENSP00000309572.5:n.2970+428C=
ENST00000334602.10:c.2781+428C=	ENSP00000334346.6:n.2781+428C=
ENST00000460137.6:c.2563+428C=	ENSP00000425003.1:n.2563+428C=
ENST00000484238.6:n.1412+428C=
NM_001193376.1:c.2781+428C=	NP_001180305.1:n.2781+428C=
NM_198253.2:c.2970+428C= , LRG_343t1:c.2970+428C=	NP_937983.2:n.2970+428C=
XM_011514104.1:c.1440+428C=	XP_011512406.1:n.1440+428C=
XM_011514105.1:c.1326+428C=	XP_011512407.1:n.1326+428C=
XM_011514106.1:c.1326+428C=	XP_011512408.1:n.1326+428C=
NR_149162.1:n.2657+428C=
NR_149163.1:n.2621+428C=
NM_001193376.2:c.2781+428C=	NP_001180305.1:n.2781+428C=
NM_198253.3:c.2970+428C= MANE Select	NP_937983.2:n.2970+428C=
NR_149162.2:n.2678+428C=
NR_149163.2:n.2642+428C=
NM_001193376.3:c.2781+428C=	NP_001180305.1:n.2781+428C=
NR_149162.3:n.2678+428C=
NR_149163.3:n.2642+428C=