Canonical Allele Identifier: CA2579846080
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295065A>C , CM000667.2:g.1295065A>C GRCh38
NC_000005.9:g.1295180A>C , CM000667.1:g.1295180A>C GRCh37
NC_000005.8:g.1348180A>C NCBI36
NG_009265.1:g.4983T>G , LRG_343:g.4983T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-76T>G MANE Select ENSP00000309572.5:n.-76T>G
ENST00000522877.1:n.5T>G
NM_001193376.2:c.-76T>G NP_001180305.1:n.-76T>G
NM_198253.3:c.-76T>G MANE Select NP_937983.2:n.-76T>G
NR_149162.2:n.4T>G
NR_149163.2:n.4T>G
NM_001193376.3:c.-76T>G NP_001180305.1:n.-76T>G
NR_149162.3:n.4T>G
NR_149163.3:n.4T>G