Canonical Allele Identifier: CA1072502551
Gene: TERT HGNC NCBI

Linked Data

dbSNP Id: rs1750470138

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1286154_1286155insTT , CM000667.2:g.1286154_1286155insTT GRCh38
NC_000005.9:g.1286269_1286270insTT , CM000667.1:g.1286269_1286270insTT GRCh37
NC_000005.8:g.1339269_1339270insTT NCBI36
NG_009265.1:g.13893_13894insAA , LRG_343:g.13893_13894insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.1574-3531_1574-3530insAA MANE Select ENSP00000309572.5:n.1574-3531_1574-3530insAA
ENST00000656021.1:c.*1119+10_*1119+11insAA ENSP00000499759.1:n.*1119+10_*1119+11insAA
ENST00000310581.9:c.1574-3531_1574-3530insAA ENSP00000309572.5:n.1574-3531_1574-3530insAA
ENST00000334602.10:c.1574-3531_1574-3530insAA ENSP00000334346.6:n.1574-3531_1574-3530insAA
ENST00000460137.6:c.1574-3531_1574-3530insAA ENSP00000425003.1:n.1574-3531_1574-3530insAA
ENST00000508104.2:c.1574-3531_1574-3530insAA ENSP00000426042.2:n.1574-3531_1574-3530insAA
NM_001193376.1:c.1574-3531_1574-3530insAA NP_001180305.1:n.1574-3531_1574-3530insAA
NM_198253.2:c.1574-3531_1574-3530insAA , LRG_343t1:c.1574-3531_1574-3530insAA NP_937983.2:n.1574-3531_1574-3530insAA
XM_011514104.1:c.43+10_43+11insAA XP_011512406.1:n.43+10_43+11insAA
XM_011514105.1:c.-103_-102insAA XP_011512407.1:n.-103_-102insAA
NR_149162.1:n.1632-3531_1632-3530insAA
NR_149163.1:n.1632-3531_1632-3530insAA
NM_001193376.2:c.1574-3531_1574-3530insAA NP_001180305.1:n.1574-3531_1574-3530insAA
NM_198253.3:c.1574-3531_1574-3530insAA MANE Select NP_937983.2:n.1574-3531_1574-3530insAA
NR_149162.2:n.1653-3531_1653-3530insAA
NR_149163.2:n.1653-3531_1653-3530insAA
NM_001193376.3:c.1574-3531_1574-3530insAA NP_001180305.1:n.1574-3531_1574-3530insAA
NR_149162.3:n.1653-3531_1653-3530insAA
NR_149163.3:n.1653-3531_1653-3530insAA