Canonical Allele Identifier: CA2673079129
Gene: TERT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1272282_1272283insCTTGAAGGCCTTGCGGACGT , CM000667.2:g.1272282_1272283insCTTGAAGGCCTTGCGGACGT GRCh38
NC_000005.9:g.1272397_1272398insCTTGAAGGCCTTGCGGACGT , CM000667.1:g.1272397_1272398insCTTGAAGGCCTTGCGGACGT GRCh37
NC_000005.8:g.1325397_1325398insCTTGAAGGCCTTGCGGACGT NCBI36
NG_009265.1:g.27766_27767insCGTCCGCAAGGCCTTCAAGA , LRG_343:g.27766_27767insCGTCCGCAAGGCCTTCAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA MANE Select ENSP00000309572.5:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
ENST00000656021.1:c.*1833-2_*1833-1insCGTCCGCAAGGCCTTCAAGA ENSP00000499759.1:n.*1833-2_*1833-1insCGTCCGCAAGGCCTTCAAGA
ENST00000310581.9:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA ENSP00000309572.5:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
ENST00000334602.10:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA ENSP00000334346.6:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
ENST00000460137.6:c.2251-3649_2251-3648insCGTCCGCAAGGCCTTCAAGA ENSP00000425003.1:n.2251-3649_2251-3648insCGTCCGCAAGGCCTTCAAG...
ENST00000484238.6:n.1100-3649_1100-3648insCGTCCGCAAGGCCTTCAAGA
ENST00000508104.2:c.2287-3649_2287-3648insCGTCCGCAAGGCCTTCAAGA ENSP00000426042.2:n.2287-3649_2287-3648insCGTCCGCAAGGCCTTCAAG...
NM_001193376.1:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA NP_001180305.1:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
NM_198253.2:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA , LRG_343t1:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA NP_937983.2:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
XM_011514104.1:c.757-2_757-1insCGTCCGCAAGGCCTTCAAGA XP_011512406.1:n.757-2_757-1insCGTCCGCAAGGCCTTCAAGA
XM_011514105.1:c.643-2_643-1insCGTCCGCAAGGCCTTCAAGA XP_011512407.1:n.643-2_643-1insCGTCCGCAAGGCCTTCAAGA
XM_011514106.1:c.643-2_643-1insCGTCCGCAAGGCCTTCAAGA XP_011512408.1:n.643-2_643-1insCGTCCGCAAGGCCTTCAAGA
NR_149162.1:n.2345-3649_2345-3648insCGTCCGCAAGGCCTTCAAGA
NR_149163.1:n.2309-3649_2309-3648insCGTCCGCAAGGCCTTCAAGA
NM_001193376.2:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA NP_001180305.1:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
NM_198253.3:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA MANE Select NP_937983.2:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
NR_149162.2:n.2366-3649_2366-3648insCGTCCGCAAGGCCTTCAAGA
NR_149163.2:n.2330-3649_2330-3648insCGTCCGCAAGGCCTTCAAGA
NM_001193376.3:c.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA NP_001180305.1:n.2287-2_2287-1insCGTCCGCAAGGCCTTCAAGA
NR_149162.3:n.2366-3649_2366-3648insCGTCCGCAAGGCCTTCAAGA
NR_149163.3:n.2330-3649_2330-3648insCGTCCGCAAGGCCTTCAAGA