Canonical Allele Identifier: CA2579846052
Gene: TERT HGNC NCBI

Linked Data

gnomAD v4: 5-1295052-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295052T>A , CM000667.2:g.1295052T>A GRCh38
NC_000005.9:g.1295167T>A , CM000667.1:g.1295167T>A GRCh37
NC_000005.8:g.1348167T>A NCBI36
NG_009265.1:g.4996A>T , LRG_343:g.4996A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-63A>T MANE Select ENSP00000309572.5:n.-63A>T
ENST00000522877.1:n.18A>T
NM_001193376.2:c.-63A>T NP_001180305.1:n.-63A>T
NM_198253.3:c.-63A>T MANE Select NP_937983.2:n.-63A>T
NR_149162.2:n.17A>T
NR_149163.2:n.17A>T
NM_001193376.3:c.-63A>T NP_001180305.1:n.-63A>T
NR_149162.3:n.17A>T
NR_149163.3:n.17A>T