Canonical Allele Identifier: CA1522539623
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260351T= , CM000667.2:g.1260351T= GRCh38
NC_000005.9:g.1260466T= , CM000667.1:g.1260466T= GRCh37
NC_000005.8:g.1313466T= NCBI36
NG_009265.1:g.39697A= , LRG_343:g.39697A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2970+123A= MANE Select ENSP00000309572.5:n.2970+123A=
ENST00000656021.1:c.*2516+123A= ENSP00000499759.1:n.*2516+123A=
ENST00000667927.1:n.258+123A=
ENST00000310581.9:c.2970+123A= ENSP00000309572.5:n.2970+123A=
ENST00000334602.10:c.2781+123A= ENSP00000334346.6:n.2781+123A=
ENST00000460137.6:c.2563+123A= ENSP00000425003.1:n.2563+123A=
ENST00000484238.6:n.1412+123A=
NM_001193376.1:c.2781+123A= NP_001180305.1:n.2781+123A=
NM_198253.2:c.2970+123A= , LRG_343t1:c.2970+123A= NP_937983.2:n.2970+123A=
XM_011514104.1:c.1440+123A= XP_011512406.1:n.1440+123A=
XM_011514105.1:c.1326+123A= XP_011512407.1:n.1326+123A=
XM_011514106.1:c.1326+123A= XP_011512408.1:n.1326+123A=
NR_149162.1:n.2657+123A=
NR_149163.1:n.2621+123A=
NM_001193376.2:c.2781+123A= NP_001180305.1:n.2781+123A=
NM_198253.3:c.2970+123A= MANE Select NP_937983.2:n.2970+123A=
NR_149162.2:n.2678+123A=
NR_149163.2:n.2642+123A=
NM_001193376.3:c.2781+123A= NP_001180305.1:n.2781+123A=
NR_149162.3:n.2678+123A=
NR_149163.3:n.2642+123A=