Canonical Allele Identifier: CA1522554945
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272264T= , CM000667.2:g.1272264T= GRCh38
NC_000005.9:g.1272379T= , CM000667.1:g.1272379T= GRCh37
NC_000005.8:g.1325379T= NCBI36
NG_009265.1:g.27784A= , LRG_343:g.27784A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2303A= MANE Select ENSP00000309572.5:p.Asp768=
ENST00000656021.1:c.*1849A= ENSP00000499759.1:n.*1849A=
ENST00000310581.9:c.2303A= ENSP00000309572.5:p.Asp768=
ENST00000334602.10:c.2303A= ENSP00000334346.6:p.Asp768=
ENST00000460137.6:c.2251-3631A= ENSP00000425003.1:n.2251-3631A=
ENST00000484238.6:n.1100-3631A=
ENST00000508104.2:c.2287-3631A= ENSP00000426042.2:n.2287-3631A=
NM_001193376.1:c.2303A= NP_001180305.1:p.Asp768=
NM_198253.2:c.2303A= , LRG_343t1:c.2303A= NP_937983.2:p.Asp768=
XM_011514104.1:c.773A= XP_011512406.1:p.Asp258=
XM_011514105.1:c.659A= XP_011512407.1:p.Asp220=
XM_011514106.1:c.659A= XP_011512408.1:p.Asp220=
NR_149162.1:n.2345-3631A=
NR_149163.1:n.2309-3631A=
NM_001193376.2:c.2303A= NP_001180305.1:p.Asp768=
NM_198253.3:c.2303A= MANE Select NP_937983.2:p.Asp768=
NR_149162.2:n.2366-3631A=
NR_149163.2:n.2330-3631A=
NM_001193376.3:c.2303A= NP_001180305.1:p.Asp768=
NR_149162.3:n.2366-3631A=
NR_149163.3:n.2330-3631A=