Canonical Allele Identifier: CA359076408

Gene: TERT

Linked Data

• ClinVar Variation Id: 1336928
• ClinVar RCV Id: RCV001819414
• dbSNP Id: rs2126617890
• MyVariant Identifiers: chr5:g.1272364A>G (hg19) ; chr5:g.1272249A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1272249A>G , CM000667.2:g.1272249A>G	GRCh38
NC_000005.9:g.1272364A>G , CM000667.1:g.1272364A>G	GRCh37
NC_000005.8:g.1325364A>G	NCBI36
NG_009265.1:g.27799T>C , LRG_343:g.27799T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2318T>C MANE Select	ENSP00000309572.5:p.Met773Thr
ENST00000656021.1:c.*1864T>C	ENSP00000499759.1:n.*1864T>C
ENST00000310581.9:c.2318T>C	ENSP00000309572.5:p.Met773Thr
ENST00000334602.10:c.2318T>C	ENSP00000334346.6:p.Met773Thr
ENST00000460137.6:c.2251-3616T>C	ENSP00000425003.1:n.2251-3616T>C
ENST00000484238.6:n.1100-3616T>C
ENST00000508104.2:c.2287-3616T>C	ENSP00000426042.2:n.2287-3616T>C
NM_001193376.1:c.2318T>C	NP_001180305.1:p.Met773Thr
NM_198253.2:c.2318T>C , LRG_343t1:c.2318T>C	NP_937983.2:p.Met773Thr
XM_011514104.1:c.788T>C	XP_011512406.1:p.Met263Thr
XM_011514105.1:c.674T>C	XP_011512407.1:p.Met225Thr
XM_011514106.1:c.674T>C	XP_011512408.1:p.Met225Thr
NR_149162.1:n.2345-3616T>C
NR_149163.1:n.2309-3616T>C
NM_001193376.2:c.2318T>C	NP_001180305.1:p.Met773Thr
NM_198253.3:c.2318T>C MANE Select	NP_937983.2:p.Met773Thr
NR_149162.2:n.2366-3616T>C
NR_149163.2:n.2330-3616T>C
NM_001193376.3:c.2318T>C	NP_001180305.1:p.Met773Thr
NR_149162.3:n.2366-3616T>C
NR_149163.3:n.2330-3616T>C