Canonical Allele Identifier: CA359079628

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278881G>C (hg19) ; chr5:g.1278766G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278766G>C , CM000667.2:g.1278766G>C	GRCh38
NC_000005.9:g.1278881G>C , CM000667.1:g.1278881G>C	GRCh37
NC_000005.8:g.1331881G>C	NCBI36
NG_009265.1:g.21282C>G , LRG_343:g.21282C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2161C>G MANE Select	ENSP00000309572.5:p.Pro721Ala
ENST00000656021.1:c.*1707C>G	ENSP00000499759.1:n.*1707C>G
ENST00000310581.9:c.2161C>G	ENSP00000309572.5:p.Pro721Ala
ENST00000334602.10:c.2161C>G	ENSP00000334346.6:p.Pro721Ala
ENST00000460137.6:c.2131-6C>G	ENSP00000425003.1:n.2131-6C>G
ENST00000484238.6:n.974C>G
ENST00000508104.2:c.2161C>G	ENSP00000426042.2:p.Pro721Ala
NM_001193376.1:c.2161C>G	NP_001180305.1:p.Pro721Ala
NM_198253.2:c.2161C>G , LRG_343t1:c.2161C>G	NP_937983.2:p.Pro721Ala
XM_011514104.1:c.631C>G	XP_011512406.1:p.Pro211Ala
XM_011514105.1:c.517C>G	XP_011512407.1:p.Pro173Ala
XM_011514106.1:c.517C>G	XP_011512408.1:p.Pro173Ala
NR_149162.1:n.2219C>G
NR_149163.1:n.2189-6C>G
NM_001193376.2:c.2161C>G	NP_001180305.1:p.Pro721Ala
NM_198253.3:c.2161C>G MANE Select	NP_937983.2:p.Pro721Ala
NR_149162.2:n.2240C>G
NR_149163.2:n.2210-6C>G
NM_001193376.3:c.2161C>G	NP_001180305.1:p.Pro721Ala
NR_149162.3:n.2240C>G
NR_149163.3:n.2210-6C>G