Canonical Allele Identifier: CA1522554925

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1272255G= , CM000667.2:g.1272255G=	GRCh38
NC_000005.9:g.1272370G= , CM000667.1:g.1272370G=	GRCh37
NC_000005.8:g.1325370G=	NCBI36
NG_009265.1:g.27793C= , LRG_343:g.27793C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2312C= MANE Select	ENSP00000309572.5:p.Pro771=
ENST00000656021.1:c.*1858C=	ENSP00000499759.1:n.*1858C=
ENST00000310581.9:c.2312C=	ENSP00000309572.5:p.Pro771=
ENST00000334602.10:c.2312C=	ENSP00000334346.6:p.Pro771=
ENST00000460137.6:c.2251-3622C=	ENSP00000425003.1:n.2251-3622C=
ENST00000484238.6:n.1100-3622C=
ENST00000508104.2:c.2287-3622C=	ENSP00000426042.2:n.2287-3622C=
NM_001193376.1:c.2312C=	NP_001180305.1:p.Pro771=
NM_198253.2:c.2312C= , LRG_343t1:c.2312C=	NP_937983.2:p.Pro771=
XM_011514104.1:c.782C=	XP_011512406.1:p.Pro261=
XM_011514105.1:c.668C=	XP_011512407.1:p.Pro223=
XM_011514106.1:c.668C=	XP_011512408.1:p.Pro223=
NR_149162.1:n.2345-3622C=
NR_149163.1:n.2309-3622C=
NM_001193376.2:c.2312C=	NP_001180305.1:p.Pro771=
NM_198253.3:c.2312C= MANE Select	NP_937983.2:p.Pro771=
NR_149162.2:n.2366-3622C=
NR_149163.2:n.2330-3622C=
NM_001193376.3:c.2312C=	NP_001180305.1:p.Pro771=
NR_149162.3:n.2366-3622C=
NR_149163.3:n.2330-3622C=