Canonical Allele Identifier: CA443005592

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1294907_1294908insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294792_1294793insC , CM000667.2:g.1294792_1294793insC	GRCh38
NC_000005.9:g.1294907_1294908insC , CM000667.1:g.1294907_1294908insC	GRCh37
NC_000005.8:g.1347907_1347908insC	NCBI36
NG_009265.1:g.5255_5256insG , LRG_343:g.5255_5256insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.197_198insG MANE Select	ENSP00000309572.5:p.Ala67ArgfsTer?
ENST00000656021.1:c.197_198insG	ENSP00000499759.1:p.Ala67ArgfsTer?
ENST00000310581.9:c.197_198insG	ENSP00000309572.5:p.Ala67ArgfsTer?
ENST00000334602.10:c.197_198insG	ENSP00000334346.6:p.Ala67ArgfsTer?
ENST00000460137.6:c.197_198insG	ENSP00000425003.1:p.Ala67ArgfsTer?
ENST00000508104.2:c.197_198insG	ENSP00000426042.2:p.Ala67ArgfsTer?
ENST00000522877.1:n.277_278insG
NM_001193376.1:c.197_198insG	NP_001180305.1:p.Ala67ArgfsTer?
NM_198253.2:c.197_198insG , LRG_343t1:c.197_198insG	NP_937983.2:p.Ala67ArgfsTer?
NR_149162.1:n.255_256insG
NR_149163.1:n.255_256insG
NM_001193376.2:c.197_198insG	NP_001180305.1:p.Ala67ArgfsTer?
NM_198253.3:c.197_198insG MANE Select	NP_937983.2:p.Ala67ArgfsTer?
NR_149162.2:n.276_277insG
NR_149163.2:n.276_277insG
NM_001193376.3:c.197_198insG	NP_001180305.1:p.Ala67ArgfsTer?
NR_149162.3:n.276_277insG
NR_149163.3:n.276_277insG