Canonical Allele Identifier: CA3184240

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1254396G>A , CM000667.2:g.1254396G>A	GRCh38
NC_000005.9:g.1254511G>A , CM000667.1:g.1254511G>A	GRCh37
NC_000005.8:g.1307511G>A	NCBI36
NG_009265.1:g.45652C>T , LRG_343:g.45652C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_198253.3:c.3267C>T MANE Select	NP_937983.2:p.Tyr1089=
ENST00000310581.10:c.3267C>T MANE Select	ENSP00000309572.5:p.Tyr1089=
NM_001193376.1:c.3078C>T	NP_001180305.1:p.Tyr1026=
NM_001193376.2:c.3078C>T	NP_001180305.1:p.Tyr1026=
NM_001193376.3:c.3078C>T	NP_001180305.1:p.Tyr1026=
NM_198253.2:c.3267C>T , LRG_343t1:c.3267C>T	NP_937983.2:p.Tyr1089=
NR_149162.1:n.2954C>T
NR_149162.2:n.2975C>T
NR_149162.3:n.2975C>T
NR_149163.1:n.2918C>T
NR_149163.2:n.2939C>T
NR_149163.3:n.2939C>T
ENST00000310581.9:c.3267C>T	ENSP00000309572.5:p.Tyr1089=
ENST00000334602.10:c.3078C>T	ENSP00000334346.6:p.Tyr1026=
ENST00000460137.6:c.2860C>T	ENSP00000425003.1:n.2860C>T
ENST00000484238.6:n.1709C>T
ENST00000656021.1:c.*2813C>T	ENSP00000499759.1:n.*2813C>T
XM_011514104.1:c.1737C>T	XP_011512406.1:p.Tyr579=
XM_011514105.1:c.1623C>T	XP_011512407.1:p.Tyr541=
XM_011514106.1:c.1623C>T	XP_011512408.1:p.Tyr541=
XR_925683.1:n.287-278G>A