Canonical Allele Identifier: CA1522555539
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1293652G= , CM000667.2:g.1293652G= GRCh38
NC_000005.9:g.1293767G= , CM000667.1:g.1293767G= GRCh37
NC_000005.8:g.1346767G= NCBI36
NG_009265.1:g.6396C= , LRG_343:g.6396C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.1234C= MANE Select ENSP00000309572.5:p.His412=
ENST00000656021.1:c.1234C= ENSP00000499759.1:p.His412=
ENST00000310581.9:c.1234C= ENSP00000309572.5:p.His412=
ENST00000334602.10:c.1234C= ENSP00000334346.6:p.His412=
ENST00000460137.6:c.1234C= ENSP00000425003.1:p.His412=
ENST00000508104.2:c.1234C= ENSP00000426042.2:p.His412=
NM_001193376.1:c.1234C= NP_001180305.1:p.His412=
NM_198253.2:c.1234C= , LRG_343t1:c.1234C= NP_937983.2:p.His412=
NR_149162.1:n.1292C=
NR_149163.1:n.1292C=
NM_001193376.2:c.1234C= NP_001180305.1:p.His412=
NM_198253.3:c.1234C= MANE Select NP_937983.2:p.His412=
NR_149162.2:n.1313C=
NR_149163.2:n.1313C=
NM_001193376.3:c.1234C= NP_001180305.1:p.His412=
NR_149162.3:n.1313C=
NR_149163.3:n.1313C=