Canonical Allele Identifier: CA1522539477

Gene: TERT

Linked Data

• dbSNP Id: rs1748124210

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260211_1260213del , CM000667.2:g.1260211_1260213del	GRCh38
NC_000005.9:g.1260326_1260328del , CM000667.1:g.1260326_1260328del	GRCh37
NC_000005.8:g.1313326_1313328del	NCBI36
NG_009265.1:g.39837_39839del , LRG_343:g.39837_39839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2970+263_2970+265del MANE Select	ENSP00000309572.5:n.2970+263_2970+265del
ENST00000656021.1:c.*2516+263_*2516+265del	ENSP00000499759.1:n.*2516+263_*2516+265del
ENST00000667927.1:n.258+263_258+265del
ENST00000310581.9:c.2970+263_2970+265del	ENSP00000309572.5:n.2970+263_2970+265del
ENST00000334602.10:c.2781+263_2781+265del	ENSP00000334346.6:n.2781+263_2781+265del
ENST00000460137.6:c.2563+263_2563+265del	ENSP00000425003.1:n.2563+263_2563+265del
ENST00000484238.6:n.1412+263_1412+265del
NM_001193376.1:c.2781+263_2781+265del	NP_001180305.1:n.2781+263_2781+265del
NM_198253.2:c.2970+263_2970+265del , LRG_343t1:c.2970+263_2970+265del	NP_937983.2:n.2970+263_2970+265del
XM_011514104.1:c.1440+263_1440+265del	XP_011512406.1:n.1440+263_1440+265del
XM_011514105.1:c.1326+263_1326+265del	XP_011512407.1:n.1326+263_1326+265del
XM_011514106.1:c.1326+263_1326+265del	XP_011512408.1:n.1326+263_1326+265del
NR_149162.1:n.2657+263_2657+265del
NR_149163.1:n.2621+263_2621+265del
NM_001193376.2:c.2781+263_2781+265del	NP_001180305.1:n.2781+263_2781+265del
NM_198253.3:c.2970+263_2970+265del MANE Select	NP_937983.2:n.2970+263_2970+265del
NR_149162.2:n.2678+263_2678+265del
NR_149163.2:n.2642+263_2642+265del
NM_001193376.3:c.2781+263_2781+265del	NP_001180305.1:n.2781+263_2781+265del
NR_149162.3:n.2678+263_2678+265del
NR_149163.3:n.2642+263_2642+265del