Canonical Allele Identifier: CA2983076171
Gene: TERT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295044_1295045insGTC , CM000667.2:g.1295044_1295045insGTC GRCh38
NC_000005.9:g.1295159_1295160insGTC , CM000667.1:g.1295159_1295160insGTC GRCh37
NC_000005.8:g.1348159_1348160insGTC NCBI36
NG_009265.1:g.5004_5005insACG , LRG_343:g.5004_5005insACG

Transcript Alleles

HGVS Amino-acid Change
NM_198253.3:c.-55_-54insACG MANE Select NP_937983.2:n.-55_-54insACG
ENST00000310581.10:c.-55_-54insACG MANE Select ENSP00000309572.5:n.-55_-54insACG
NM_001193376.1:c.-55_-54insACG NP_001180305.1:n.-55_-54insACG
NM_001193376.2:c.-55_-54insACG NP_001180305.1:n.-55_-54insACG
NM_001193376.3:c.-55_-54insACG NP_001180305.1:n.-55_-54insACG
NM_198253.2:c.-55_-54insACG , LRG_343t1:c.-55_-54insACG NP_937983.2:n.-55_-54insACG
NR_149162.1:n.4_5insACG
NR_149162.2:n.25_26insACG
NR_149162.3:n.25_26insACG
NR_149163.1:n.4_5insACG
NR_149163.2:n.25_26insACG
NR_149163.3:n.25_26insACG
ENST00000310581.9:c.-55_-54insACG ENSP00000309572.5:n.-55_-54insACG
ENST00000522877.1:n.26_27insACG
ENST00000656021.1:c.-55_-54insACG ENSP00000499759.1:n.-55_-54insACG
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