Canonical Allele Identifier: CA1522534675

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1255401A= , CM000667.2:g.1255401A=	GRCh38
NC_000005.9:g.1255516A= , CM000667.1:g.1255516A=	GRCh37
NC_000005.8:g.1308516A=	NCBI36
NG_009265.1:g.44647T= , LRG_343:g.44647T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.3043T= MANE Select	ENSP00000309572.5:p.Cys1015=
ENST00000656021.1:c.*2589T=	ENSP00000499759.1:n.*2589T=
ENST00000667927.1:n.331T=
ENST00000310581.9:c.3043T=	ENSP00000309572.5:p.Cys1015=
ENST00000334602.10:c.2854T=	ENSP00000334346.6:p.Cys952=
ENST00000460137.6:c.2636T=	ENSP00000425003.1:n.2636T=
ENST00000484238.6:n.1485T=
NM_001193376.1:c.2854T=	NP_001180305.1:p.Cys952=
NM_198253.2:c.3043T= , LRG_343t1:c.3043T=	NP_937983.2:p.Cys1015=
XM_011514104.1:c.1513T=	XP_011512406.1:p.Cys505=
XM_011514105.1:c.1399T=	XP_011512407.1:p.Cys467=
XM_011514106.1:c.1399T=	XP_011512408.1:p.Cys467=
NR_149162.1:n.2730T=
NR_149163.1:n.2694T=
NM_001193376.2:c.2854T=	NP_001180305.1:p.Cys952=
NM_198253.3:c.3043T= MANE Select	NP_937983.2:p.Cys1015=
NR_149162.2:n.2751T=
NR_149163.2:n.2715T=
NM_001193376.3:c.2854T=	NP_001180305.1:p.Cys952=
NR_149162.3:n.2751T=
NR_149163.3:n.2715T=