Canonical Allele Identifier: CA112930155
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs923465553

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1260417_1260418del , CM000667.2:g.1260417_1260418del GRCh38
NC_000005.9:g.1260532_1260533del , CM000667.1:g.1260532_1260533del GRCh37
NC_000005.8:g.1313532_1313533del NCBI36
NG_009265.1:g.39631_39632del , LRG_343:g.39631_39632del

Transcript Alleles

HGVS Amino-acid change
ENST00000310581.10:c.2970+57_2970+58del MANE Select ENSP00000309572.5:n.2970+57_2970+58del
ENST00000656021.1:c.*2516+57_*2516+58del ENSP00000499759.1:n.*2516+57_*2516+58del
ENST00000667927.1:n.258+57_258+58del
ENST00000310581.9:c.2970+57_2970+58del ENSP00000309572.5:n.2970+57_2970+58del
ENST00000334602.10:c.2781+57_2781+58del ENSP00000334346.6:n.2781+57_2781+58del
ENST00000460137.6:c.2563+57_2563+58del ENSP00000425003.1:n.2563+57_2563+58del
ENST00000484238.6:n.1412+57_1412+58del
NM_001193376.1:c.2781+57_2781+58del NP_001180305.1:n.2781+57_2781+58del
NM_198253.2:c.2970+57_2970+58del , LRG_343t1:c.2970+57_2970+58del NP_937983.2:n.2970+57_2970+58del
XM_011514104.1:c.1440+57_1440+58del XP_011512406.1:n.1440+57_1440+58del
XM_011514105.1:c.1326+57_1326+58del XP_011512407.1:n.1326+57_1326+58del
XM_011514106.1:c.1326+57_1326+58del XP_011512408.1:n.1326+57_1326+58del
NR_149162.1:n.2657+57_2657+58del
NR_149163.1:n.2621+57_2621+58del
NM_001193376.2:c.2781+57_2781+58del NP_001180305.1:n.2781+57_2781+58del
NM_198253.3:c.2970+57_2970+58del MANE Select NP_937983.2:n.2970+57_2970+58del
NR_149162.2:n.2678+57_2678+58del
NR_149163.2:n.2642+57_2642+58del
NM_001193376.3:c.2781+57_2781+58del NP_001180305.1:n.2781+57_2781+58del
NR_149162.3:n.2678+57_2678+58del
NR_149163.3:n.2642+57_2642+58del