Canonical Allele Identifier: CA2578259829
Gene: TERT HGNC NCBI

Linked Data

gnomAD v4: 5-1295059-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295059G>T , CM000667.2:g.1295059G>T GRCh38
NC_000005.9:g.1295174G>T , CM000667.1:g.1295174G>T GRCh37
NC_000005.8:g.1348174G>T NCBI36
NG_009265.1:g.4989C>A , LRG_343:g.4989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-70C>A MANE Select ENSP00000309572.5:n.-70C>A
ENST00000522877.1:n.11C>A
NM_001193376.2:c.-70C>A NP_001180305.1:n.-70C>A
NM_198253.3:c.-70C>A MANE Select NP_937983.2:n.-70C>A
NR_149162.2:n.10C>A
NR_149163.2:n.10C>A
NM_001193376.3:c.-70C>A NP_001180305.1:n.-70C>A
NR_149162.3:n.10C>A
NR_149163.3:n.10C>A