Canonical Allele Identifier: CA803362130

Gene: TERT

Linked Data

• dbSNP Id: rs1432439617
• MyVariant Identifiers: chr5:g.1260329_1260330del (hg19) ; chr5:g.1260214_1260215del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260216_1260217del , CM000667.2:g.1260216_1260217del	GRCh38
NC_000005.9:g.1260331_1260332del , CM000667.1:g.1260331_1260332del	GRCh37
NC_000005.8:g.1313331_1313332del	NCBI36
NG_009265.1:g.39833_39834del , LRG_343:g.39833_39834del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+259_2970+260del MANE Select	ENSP00000309572.5:n.2970+259_2970+260del
ENST00000656021.1:c.*2516+259_*2516+260del	ENSP00000499759.1:n.*2516+259_*2516+260del
ENST00000667927.1:n.258+259_258+260del
ENST00000310581.9:c.2970+259_2970+260del	ENSP00000309572.5:n.2970+259_2970+260del
ENST00000334602.10:c.2781+259_2781+260del	ENSP00000334346.6:n.2781+259_2781+260del
ENST00000460137.6:c.2563+259_2563+260del	ENSP00000425003.1:n.2563+259_2563+260del
ENST00000484238.6:n.1412+259_1412+260del
NM_001193376.1:c.2781+259_2781+260del	NP_001180305.1:n.2781+259_2781+260del
NM_198253.2:c.2970+259_2970+260del , LRG_343t1:c.2970+259_2970+260del	NP_937983.2:n.2970+259_2970+260del
XM_011514104.1:c.1440+259_1440+260del	XP_011512406.1:n.1440+259_1440+260del
XM_011514105.1:c.1326+259_1326+260del	XP_011512407.1:n.1326+259_1326+260del
XM_011514106.1:c.1326+259_1326+260del	XP_011512408.1:n.1326+259_1326+260del
NR_149162.1:n.2657+259_2657+260del
NR_149163.1:n.2621+259_2621+260del
NM_001193376.2:c.2781+259_2781+260del	NP_001180305.1:n.2781+259_2781+260del
NM_198253.3:c.2970+259_2970+260del MANE Select	NP_937983.2:n.2970+259_2970+260del
NR_149162.2:n.2678+259_2678+260del
NR_149163.2:n.2642+259_2642+260del
NM_001193376.3:c.2781+259_2781+260del	NP_001180305.1:n.2781+259_2781+260del
NR_149162.3:n.2678+259_2678+260del
NR_149163.3:n.2642+259_2642+260del