Canonical Allele Identifier: CA803362202

Gene: TERT

Linked Data

• dbSNP Id: rs1167267909
• gnomAD v3: 5-1260337-T-A
• gnomAD v4: 5-1260337-T-A
• MyVariant Identifiers: chr5:g.1260452T>A (hg19) ; chr5:g.1260337T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260337T>A , CM000667.2:g.1260337T>A	GRCh38
NC_000005.9:g.1260452T>A , CM000667.1:g.1260452T>A	GRCh37
NC_000005.8:g.1313452T>A	NCBI36
NG_009265.1:g.39711A>T , LRG_343:g.39711A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2970+137A>T MANE Select	ENSP00000309572.5:n.2970+137A>T
ENST00000656021.1:c.*2516+137A>T	ENSP00000499759.1:n.*2516+137A>T
ENST00000667927.1:n.258+137A>T
ENST00000310581.9:c.2970+137A>T	ENSP00000309572.5:n.2970+137A>T
ENST00000334602.10:c.2781+137A>T	ENSP00000334346.6:n.2781+137A>T
ENST00000460137.6:c.2563+137A>T	ENSP00000425003.1:n.2563+137A>T
ENST00000484238.6:n.1412+137A>T
NM_001193376.1:c.2781+137A>T	NP_001180305.1:n.2781+137A>T
NM_198253.2:c.2970+137A>T , LRG_343t1:c.2970+137A>T	NP_937983.2:n.2970+137A>T
XM_011514104.1:c.1440+137A>T	XP_011512406.1:n.1440+137A>T
XM_011514105.1:c.1326+137A>T	XP_011512407.1:n.1326+137A>T
XM_011514106.1:c.1326+137A>T	XP_011512408.1:n.1326+137A>T
NR_149162.1:n.2657+137A>T
NR_149163.1:n.2621+137A>T
NM_001193376.2:c.2781+137A>T	NP_001180305.1:n.2781+137A>T
NM_198253.3:c.2970+137A>T MANE Select	NP_937983.2:n.2970+137A>T
NR_149162.2:n.2678+137A>T
NR_149163.2:n.2642+137A>T
NM_001193376.3:c.2781+137A>T	NP_001180305.1:n.2781+137A>T
NR_149162.3:n.2678+137A>T
NR_149163.3:n.2642+137A>T