Canonical Allele Identifier: CA1522559357
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1751308706
gnomAD v4: 5-1295037-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295037A>T , CM000667.2:g.1295037A>T GRCh38
NC_000005.9:g.1295152A>T , CM000667.1:g.1295152A>T GRCh37
NC_000005.8:g.1348152A>T NCBI36
NG_009265.1:g.5011T>A , LRG_343:g.5011T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-48T>A MANE Select ENSP00000309572.5:n.-48T>A
ENST00000656021.1:c.-48T>A ENSP00000499759.1:n.-48T>A
ENST00000310581.9:c.-48T>A ENSP00000309572.5:n.-48T>A
ENST00000522877.1:n.33T>A
NM_001193376.1:c.-48T>A NP_001180305.1:n.-48T>A
NM_198253.2:c.-48T>A , LRG_343t1:c.-48T>A NP_937983.2:n.-48T>A
NR_149162.1:n.11T>A
NR_149163.1:n.11T>A
NM_001193376.2:c.-48T>A NP_001180305.1:n.-48T>A
NM_198253.3:c.-48T>A MANE Select NP_937983.2:n.-48T>A
NR_149162.2:n.32T>A
NR_149163.2:n.32T>A
NM_001193376.3:c.-48T>A NP_001180305.1:n.-48T>A
NR_149162.3:n.32T>A
NR_149163.3:n.32T>A