Canonical Allele Identifier: CA1522574670

Gene: TERT

Linked Data

• dbSNP Id: rs1750483832

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1286345T>G , CM000667.2:g.1286345T>G	GRCh38
NC_000005.9:g.1286460T>G , CM000667.1:g.1286460T>G	GRCh37
NC_000005.8:g.1339460T>G	NCBI36
NG_009265.1:g.13703A>C , LRG_343:g.13703A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.1574-3721A>C MANE Select	ENSP00000309572.5:n.1574-3721A>C
ENST00000656021.1:c.*939A>C	ENSP00000499759.1:n.*939A>C
ENST00000310581.9:c.1574-3721A>C	ENSP00000309572.5:n.1574-3721A>C
ENST00000334602.10:c.1574-3721A>C	ENSP00000334346.6:n.1574-3721A>C
ENST00000460137.6:c.1574-3721A>C	ENSP00000425003.1:n.1574-3721A>C
ENST00000508104.2:c.1574-3721A>C	ENSP00000426042.2:n.1574-3721A>C
NM_001193376.1:c.1574-3721A>C	NP_001180305.1:n.1574-3721A>C
NM_198253.2:c.1574-3721A>C , LRG_343t1:c.1574-3721A>C	NP_937983.2:n.1574-3721A>C
XM_011514104.1:c.-138A>C	XP_011512406.1:n.-138A>C
XM_011514105.1:c.-293A>C	XP_011512407.1:n.-293A>C
NR_149162.1:n.1632-3721A>C
NR_149163.1:n.1632-3721A>C
NM_001193376.2:c.1574-3721A>C	NP_001180305.1:n.1574-3721A>C
NM_198253.3:c.1574-3721A>C MANE Select	NP_937983.2:n.1574-3721A>C
NR_149162.2:n.1653-3721A>C
NR_149163.2:n.1653-3721A>C
NM_001193376.3:c.1574-3721A>C	NP_001180305.1:n.1574-3721A>C
NR_149162.3:n.1653-3721A>C
NR_149163.3:n.1653-3721A>C