Canonical Allele Identifier: CA1522559363
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295040G= , CM000667.2:g.1295040G= GRCh38
NC_000005.9:g.1295155G= , CM000667.1:g.1295155G= GRCh37
NC_000005.8:g.1348155G= NCBI36
NG_009265.1:g.5008C= , LRG_343:g.5008C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-51C= MANE Select ENSP00000309572.5:n.-51C=
ENST00000656021.1:c.-51C= ENSP00000499759.1:n.-51C=
ENST00000310581.9:c.-51C= ENSP00000309572.5:n.-51C=
ENST00000522877.1:n.30C=
NM_001193376.1:c.-51C= NP_001180305.1:n.-51C=
NM_198253.2:c.-51C= , LRG_343t1:c.-51C= NP_937983.2:n.-51C=
NR_149162.1:n.8C=
NR_149163.1:n.8C=
NM_001193376.2:c.-51C= NP_001180305.1:n.-51C=
NM_198253.3:c.-51C= MANE Select NP_937983.2:n.-51C=
NR_149162.2:n.29C=
NR_149163.2:n.29C=
NM_001193376.3:c.-51C= NP_001180305.1:n.-51C=
NR_149162.3:n.29C=
NR_149163.3:n.29C=