Canonical Allele Identifier: CA359073078

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1266580T>G (hg19) ; chr5:g.1266465T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266465T>G , CM000667.2:g.1266465T>G	GRCh38
NC_000005.9:g.1266580T>G , CM000667.1:g.1266580T>G	GRCh37
NC_000005.8:g.1319580T>G	NCBI36
NG_009265.1:g.33583A>C , LRG_343:g.33583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2653A>C MANE Select	ENSP00000309572.5:p.Arg885=
ENST00000656021.1:c.*2199A>C	ENSP00000499759.1:n.*2199A>C
ENST00000310581.9:c.2653A>C	ENSP00000309572.5:p.Arg885=
ENST00000334602.10:c.2653A>C	ENSP00000334346.6:p.Ser885Arg
ENST00000460137.6:c.2435A>C	ENSP00000425003.1:n.2435A>C
ENST00000484238.6:n.1284A>C
ENST00000503656.1:n.60A>C
ENST00000508104.2:c.2471A>C	ENSP00000426042.2:n.2471A>C
NM_001193376.1:c.2653A>C	NP_001180305.1:p.Ser885Arg
NM_198253.2:c.2653A>C , LRG_343t1:c.2653A>C	NP_937983.2:p.Arg885=
XM_011514104.1:c.1123A>C	XP_011512406.1:p.Arg375=
XM_011514105.1:c.1009A>C	XP_011512407.1:p.Arg337=
XM_011514106.1:c.1009A>C	XP_011512408.1:p.Arg337=
NR_149162.1:n.2529A>C
NR_149163.1:n.2493A>C
NM_001193376.2:c.2653A>C	NP_001180305.1:p.Ser885Arg
NM_198253.3:c.2653A>C MANE Select	NP_937983.2:p.Arg885=
NR_149162.2:n.2550A>C
NR_149163.2:n.2514A>C
NM_001193376.3:c.2653A>C	NP_001180305.1:p.Ser885Arg
NR_149162.3:n.2550A>C
NR_149163.3:n.2514A>C