Canonical Allele Identifier: CA359079324

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278833T>A (hg19) ; chr5:g.1278718T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278718T>A , CM000667.2:g.1278718T>A	GRCh38
NC_000005.9:g.1278833T>A , CM000667.1:g.1278833T>A	GRCh37
NC_000005.8:g.1331833T>A	NCBI36
NG_009265.1:g.21330A>T , LRG_343:g.21330A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2209A>T MANE Select	ENSP00000309572.5:p.Asn737Tyr
ENST00000656021.1:c.*1755A>T	ENSP00000499759.1:n.*1755A>T
ENST00000310581.9:c.2209A>T	ENSP00000309572.5:p.Asn737Tyr
ENST00000334602.10:c.2209A>T	ENSP00000334346.6:p.Asn737Tyr
ENST00000460137.6:c.2173A>T	ENSP00000425003.1:p.Asn725Tyr
ENST00000484238.6:n.1022A>T
ENST00000508104.2:c.2209A>T	ENSP00000426042.2:p.Asn737Tyr
NM_001193376.1:c.2209A>T	NP_001180305.1:p.Asn737Tyr
NM_198253.2:c.2209A>T , LRG_343t1:c.2209A>T	NP_937983.2:p.Asn737Tyr
XM_011514104.1:c.679A>T	XP_011512406.1:p.Asn227Tyr
XM_011514105.1:c.565A>T	XP_011512407.1:p.Asn189Tyr
XM_011514106.1:c.565A>T	XP_011512408.1:p.Asn189Tyr
NR_149162.1:n.2267A>T
NR_149163.1:n.2231A>T
NM_001193376.2:c.2209A>T	NP_001180305.1:p.Asn737Tyr
NM_198253.3:c.2209A>T MANE Select	NP_937983.2:p.Asn737Tyr
NR_149162.2:n.2288A>T
NR_149163.2:n.2252A>T
NM_001193376.3:c.2209A>T	NP_001180305.1:p.Asn737Tyr
NR_149162.3:n.2288A>T
NR_149163.3:n.2252A>T