Canonical Allele Identifier: CA803534492

Gene: TERT

Linked Data

• dbSNP Id: rs1400465269
• MyVariant Identifiers: chr5:g.1275905_1275906insAAAACCAACTCCACAGATCCCCACCTACCCCCACACATA (hg19) ; chr5:g.1275790_1275791insAAAACCAACTCCACAGATCCCCACCTACCCCCACACATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1275821_1275822insCACACATAAAAACCAACTCCACAGATCCCCACCTACCCC , CM000667.2:g.1275821_1275822insCACACATAAAAACCAACTCCACAGATCCCCACCTACCCC	GRCh38
NC_000005.9:g.1275936_1275937insCACACATAAAAACCAACTCCACAGATCCCCACCTACCCC , CM000667.1:g.1275936_1275937insCACACATAAAAACCAACTCCACAGATCCCCACCTACCCC	GRCh37
NC_000005.8:g.1328936_1328937insCACACATAAAAACCAACTCCACAGATCCCCACCTACCCC	NCBI36
NG_009265.1:g.24257_24258insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT , LRG_343:g.24257_24258insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT MANE Select	ENSP00000309572.5:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGG...
ENST00000656021.1:c.*1832+2850_*1832+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	ENSP00000499759.1:n.*1832+2850_*1832+2851insTATGTGTGGGGGTAGGT...
ENST00000310581.9:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	ENSP00000309572.5:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGG...
ENST00000334602.10:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	ENSP00000334346.6:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGG...
ENST00000460137.6:c.2250+2850_2250+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	ENSP00000425003.1:n.2250+2850_2250+2851insTATGTGTGGGGGTAGGTGG...
ENST00000484238.6:n.1099+2850_1099+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
ENST00000508104.2:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	ENSP00000426042.2:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGG...
NM_001193376.1:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	NP_001180305.1:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGA...
NM_198253.2:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT , LRG_343t1:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	NP_937983.2:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCT...
XM_011514104.1:c.756+2850_756+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	XP_011512406.1:n.756+2850_756+2851insTATGTGTGGGGGTAGGTGGGGATC...
XM_011514105.1:c.642+2850_642+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	XP_011512407.1:n.642+2850_642+2851insTATGTGTGGGGGTAGGTGGGGATC...
XM_011514106.1:c.642+2850_642+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	XP_011512408.1:n.642+2850_642+2851insTATGTGTGGGGGTAGGTGGGGATC...
NR_149162.1:n.2344+2850_2344+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
NR_149163.1:n.2308+2850_2308+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
NM_001193376.2:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	NP_001180305.1:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGA...
NM_198253.3:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT MANE Select	NP_937983.2:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCT...
NR_149162.2:n.2365+2850_2365+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
NR_149163.2:n.2329+2850_2329+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
NM_001193376.3:c.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT	NP_001180305.1:n.2286+2850_2286+2851insTATGTGTGGGGGTAGGTGGGGA...
NR_149162.3:n.2365+2850_2365+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT
NR_149163.3:n.2329+2850_2329+2851insTATGTGTGGGGGTAGGTGGGGATCTGTGGAGTTGGTTTT