Canonical Allele Identifier: CA443021902

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266472G>C , CM000667.2:g.1266472G>C	GRCh38
NC_000005.9:g.1266587G>C , CM000667.1:g.1266587G>C	GRCh37
NC_000005.8:g.1319587G>C	NCBI36
NG_009265.1:g.33576C>G , LRG_343:g.33576C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198253.3:c.2646C>G MANE Select	NP_937983.2:p.Thr882=
ENST00000310581.10:c.2646C>G MANE Select	ENSP00000309572.5:p.Thr882=
NM_001193376.1:c.2646C>G	NP_001180305.1:p.Thr882=
NM_001193376.2:c.2646C>G	NP_001180305.1:p.Thr882=
NM_001193376.3:c.2646C>G	NP_001180305.1:p.Thr882=
NM_198253.2:c.2646C>G , LRG_343t1:c.2646C>G	NP_937983.2:p.Thr882=
NR_149162.1:n.2522C>G
NR_149162.2:n.2543C>G
NR_149162.3:n.2543C>G
NR_149163.1:n.2486C>G
NR_149163.2:n.2507C>G
NR_149163.3:n.2507C>G
ENST00000310581.9:c.2646C>G	ENSP00000309572.5:p.Thr882=
ENST00000334602.10:c.2646C>G	ENSP00000334346.6:p.Thr882=
ENST00000460137.6:c.2428C>G	ENSP00000425003.1:n.2428C>G
ENST00000484238.6:n.1277C>G
ENST00000503656.1:n.53C>G
ENST00000508104.2:c.2464C>G	ENSP00000426042.2:n.2464C>G
ENST00000656021.1:c.*2192C>G	ENSP00000499759.1:n.*2192C>G
XM_011514104.1:c.1116C>G	XP_011512406.1:p.Thr372=
XM_011514105.1:c.1002C>G	XP_011512407.1:p.Thr334=
XM_011514106.1:c.1002C>G	XP_011512408.1:p.Thr334=