Canonical Allele Identifier: CA2573138562

Gene: TERT

Linked Data

• ClinVar Variation Id: 1591310
• ClinVar RCV Id: RCV003015305
• dbSNP Id: rs2126618123
• gnomAD v4: 5-1272290-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1272290G>A , CM000667.2:g.1272290G>A	GRCh38
NC_000005.9:g.1272405G>A , CM000667.1:g.1272405G>A	GRCh37
NC_000005.8:g.1325405G>A	NCBI36
NG_009265.1:g.27758C>T , LRG_343:g.27758C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2287-10C>T MANE Select	ENSP00000309572.5:n.2287-10C>T
ENST00000656021.1:c.*1833-10C>T	ENSP00000499759.1:n.*1833-10C>T
ENST00000310581.9:c.2287-10C>T	ENSP00000309572.5:n.2287-10C>T
ENST00000334602.10:c.2287-10C>T	ENSP00000334346.6:n.2287-10C>T
ENST00000460137.6:c.2251-3657C>T	ENSP00000425003.1:n.2251-3657C>T
ENST00000484238.6:n.1100-3657C>T
ENST00000508104.2:c.2287-3657C>T	ENSP00000426042.2:n.2287-3657C>T
NM_001193376.1:c.2287-10C>T	NP_001180305.1:n.2287-10C>T
NM_198253.2:c.2287-10C>T , LRG_343t1:c.2287-10C>T	NP_937983.2:n.2287-10C>T
XM_011514104.1:c.757-10C>T	XP_011512406.1:n.757-10C>T
XM_011514105.1:c.643-10C>T	XP_011512407.1:n.643-10C>T
XM_011514106.1:c.643-10C>T	XP_011512408.1:n.643-10C>T
NR_149162.1:n.2345-3657C>T
NR_149163.1:n.2309-3657C>T
NM_001193376.2:c.2287-10C>T	NP_001180305.1:n.2287-10C>T
NM_198253.3:c.2287-10C>T MANE Select	NP_937983.2:n.2287-10C>T
NR_149162.2:n.2366-3657C>T
NR_149163.2:n.2330-3657C>T
NM_001193376.3:c.2287-10C>T	NP_001180305.1:n.2287-10C>T
NR_149162.3:n.2366-3657C>T
NR_149163.3:n.2330-3657C>T