Canonical Allele Identifier: CA2579846026
Gene: TERT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295040G>C , CM000667.2:g.1295040G>C GRCh38
NC_000005.9:g.1295155G>C , CM000667.1:g.1295155G>C GRCh37
NC_000005.8:g.1348155G>C NCBI36
NG_009265.1:g.5008C>G , LRG_343:g.5008C>G

Transcript Alleles

HGVS Amino-acid Change
NM_198253.3:c.-51C>G MANE Select NP_937983.2:n.-51C>G
ENST00000310581.10:c.-51C>G MANE Select ENSP00000309572.5:n.-51C>G
NM_001193376.1:c.-51C>G NP_001180305.1:n.-51C>G
NM_001193376.2:c.-51C>G NP_001180305.1:n.-51C>G
NM_001193376.3:c.-51C>G NP_001180305.1:n.-51C>G
NM_198253.2:c.-51C>G , LRG_343t1:c.-51C>G NP_937983.2:n.-51C>G
NR_149162.1:n.8C>G
NR_149162.2:n.29C>G
NR_149162.3:n.29C>G
NR_149163.1:n.8C>G
NR_149163.2:n.29C>G
NR_149163.3:n.29C>G
ENST00000310581.9:c.-51C>G ENSP00000309572.5:n.-51C>G
ENST00000522877.1:n.30C>G
ENST00000656021.1:c.-51C>G ENSP00000499759.1:n.-51C>G
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