Canonical Allele Identifier: CA1522545622

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266478C= , CM000667.2:g.1266478C=	GRCh38
NC_000005.9:g.1266593C= , CM000667.1:g.1266593C=	GRCh37
NC_000005.8:g.1319593C=	NCBI36
NG_009265.1:g.33570G= , LRG_343:g.33570G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2640G= MANE Select	ENSP00000309572.5:p.Ala880=
ENST00000656021.1:c.*2186G=	ENSP00000499759.1:n.*2186G=
ENST00000310581.9:c.2640G=	ENSP00000309572.5:p.Ala880=
ENST00000334602.10:c.2640G=	ENSP00000334346.6:p.Ala880=
ENST00000460137.6:c.2422G=	ENSP00000425003.1:n.2422G=
ENST00000484238.6:n.1271G=
ENST00000503656.1:n.47G=
ENST00000508104.2:c.2458G=	ENSP00000426042.2:n.2458G=
NM_001193376.1:c.2640G=	NP_001180305.1:p.Ala880=
NM_198253.2:c.2640G= , LRG_343t1:c.2640G=	NP_937983.2:p.Ala880=
XM_011514104.1:c.1110G=	XP_011512406.1:p.Ala370=
XM_011514105.1:c.996G=	XP_011512407.1:p.Ala332=
XM_011514106.1:c.996G=	XP_011512408.1:p.Ala332=
NR_149162.1:n.2516G=
NR_149163.1:n.2480G=
NM_001193376.2:c.2640G=	NP_001180305.1:p.Ala880=
NM_198253.3:c.2640G= MANE Select	NP_937983.2:p.Ala880=
NR_149162.2:n.2537G=
NR_149163.2:n.2501G=
NM_001193376.3:c.2640G=	NP_001180305.1:p.Ala880=
NR_149162.3:n.2537G=
NR_149163.3:n.2501G=