Canonical Allele Identifier: CA803362242

Gene: TERT

Linked Data

• dbSNP Id: rs1554038790
• MyVariant Identifiers: chr5:g.1260509_1260510insTGCG (hg19) ; chr5:g.1260394_1260395insTGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260394_1260395insTGCG , CM000667.2:g.1260394_1260395insTGCG	GRCh38
NC_000005.9:g.1260509_1260510insTGCG , CM000667.1:g.1260509_1260510insTGCG	GRCh37
NC_000005.8:g.1313509_1313510insTGCG	NCBI36
NG_009265.1:g.39653_39654insCGCA , LRG_343:g.39653_39654insCGCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+79_2970+80insCGCA MANE Select	ENSP00000309572.5:n.2970+79_2970+80insCGCA
ENST00000656021.1:c.*2516+79_*2516+80insCGCA	ENSP00000499759.1:n.*2516+79_*2516+80insCGCA
ENST00000667927.1:n.258+79_258+80insCGCA
ENST00000310581.9:c.2970+79_2970+80insCGCA	ENSP00000309572.5:n.2970+79_2970+80insCGCA
ENST00000334602.10:c.2781+79_2781+80insCGCA	ENSP00000334346.6:n.2781+79_2781+80insCGCA
ENST00000460137.6:c.2563+79_2563+80insCGCA	ENSP00000425003.1:n.2563+79_2563+80insCGCA
ENST00000484238.6:n.1412+79_1412+80insCGCA
NM_001193376.1:c.2781+79_2781+80insCGCA	NP_001180305.1:n.2781+79_2781+80insCGCA
NM_198253.2:c.2970+79_2970+80insCGCA , LRG_343t1:c.2970+79_2970+80insCGCA	NP_937983.2:n.2970+79_2970+80insCGCA
XM_011514104.1:c.1440+79_1440+80insCGCA	XP_011512406.1:n.1440+79_1440+80insCGCA
XM_011514105.1:c.1326+79_1326+80insCGCA	XP_011512407.1:n.1326+79_1326+80insCGCA
XM_011514106.1:c.1326+79_1326+80insCGCA	XP_011512408.1:n.1326+79_1326+80insCGCA
NR_149162.1:n.2657+79_2657+80insCGCA
NR_149163.1:n.2621+79_2621+80insCGCA
NM_001193376.2:c.2781+79_2781+80insCGCA	NP_001180305.1:n.2781+79_2781+80insCGCA
NM_198253.3:c.2970+79_2970+80insCGCA MANE Select	NP_937983.2:n.2970+79_2970+80insCGCA
NR_149162.2:n.2678+79_2678+80insCGCA
NR_149163.2:n.2642+79_2642+80insCGCA
NM_001193376.3:c.2781+79_2781+80insCGCA	NP_001180305.1:n.2781+79_2781+80insCGCA
NR_149162.3:n.2678+79_2678+80insCGCA
NR_149163.3:n.2642+79_2642+80insCGCA