Canonical Allele Identifier: CA359069702
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260494T>A , CM000667.2:g.1260494T>A GRCh38
NC_000005.9:g.1260609T>A , CM000667.1:g.1260609T>A GRCh37
NC_000005.8:g.1313609T>A NCBI36
NG_009265.1:g.39554A>T , LRG_343:g.39554A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2950A>T MANE Select ENSP00000309572.5:p.Ser984Cys
ENST00000656021.1:c.*2496A>T ENSP00000499759.1:n.*2496A>T
ENST00000667927.1:n.238A>T
ENST00000310581.9:c.2950A>T ENSP00000309572.5:p.Ser984Cys
ENST00000334602.10:c.2761A>T ENSP00000334346.6:p.Ser921Cys
ENST00000460137.6:c.2543A>T ENSP00000425003.1:n.2543A>T
ENST00000484238.6:n.1392A>T
NM_001193376.1:c.2761A>T NP_001180305.1:p.Ser921Cys
NM_198253.2:c.2950A>T , LRG_343t1:c.2950A>T NP_937983.2:p.Ser984Cys
XM_011514104.1:c.1420A>T XP_011512406.1:p.Ser474Cys
XM_011514105.1:c.1306A>T XP_011512407.1:p.Ser436Cys
XM_011514106.1:c.1306A>T XP_011512408.1:p.Ser436Cys
NR_149162.1:n.2637A>T
NR_149163.1:n.2601A>T
NM_001193376.2:c.2761A>T NP_001180305.1:p.Ser921Cys
NM_198253.3:c.2950A>T MANE Select NP_937983.2:p.Ser984Cys
NR_149162.2:n.2658A>T
NR_149163.2:n.2622A>T
NM_001193376.3:c.2761A>T NP_001180305.1:p.Ser921Cys
NR_149162.3:n.2658A>T
NR_149163.3:n.2622A>T