Canonical Allele Identifier: CA1522539786

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260491G= , CM000667.2:g.1260491G=	GRCh38
NC_000005.9:g.1260606G= , CM000667.1:g.1260606G=	GRCh37
NC_000005.8:g.1313606G=	NCBI36
NG_009265.1:g.39557C= , LRG_343:g.39557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2953C= MANE Select	ENSP00000309572.5:p.Leu985=
ENST00000656021.1:c.*2499C=	ENSP00000499759.1:n.*2499C=
ENST00000667927.1:n.241C=
ENST00000310581.9:c.2953C=	ENSP00000309572.5:p.Leu985=
ENST00000334602.10:c.2764C=	ENSP00000334346.6:p.Leu922=
ENST00000460137.6:c.2546C=	ENSP00000425003.1:n.2546C=
ENST00000484238.6:n.1395C=
NM_001193376.1:c.2764C=	NP_001180305.1:p.Leu922=
NM_198253.2:c.2953C= , LRG_343t1:c.2953C=	NP_937983.2:p.Leu985=
XM_011514104.1:c.1423C=	XP_011512406.1:p.Leu475=
XM_011514105.1:c.1309C=	XP_011512407.1:p.Leu437=
XM_011514106.1:c.1309C=	XP_011512408.1:p.Leu437=
NR_149162.1:n.2640C=
NR_149163.1:n.2604C=
NM_001193376.2:c.2764C=	NP_001180305.1:p.Leu922=
NM_198253.3:c.2953C= MANE Select	NP_937983.2:p.Leu985=
NR_149162.2:n.2661C=
NR_149163.2:n.2625C=
NM_001193376.3:c.2764C=	NP_001180305.1:p.Leu922=
NR_149162.3:n.2661C=
NR_149163.3:n.2625C=