Canonical Allele Identifier: CA359069588

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1260596T>C (hg19) ; chr5:g.1260481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260481T>C , CM000667.2:g.1260481T>C	GRCh38
NC_000005.9:g.1260596T>C , CM000667.1:g.1260596T>C	GRCh37
NC_000005.8:g.1313596T>C	NCBI36
NG_009265.1:g.39567A>G , LRG_343:g.39567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2963A>G MANE Select	ENSP00000309572.5:p.Asp988Gly
ENST00000656021.1:c.*2509A>G	ENSP00000499759.1:n.*2509A>G
ENST00000667927.1:n.251A>G
ENST00000310581.9:c.2963A>G	ENSP00000309572.5:p.Asp988Gly
ENST00000334602.10:c.2774A>G	ENSP00000334346.6:p.Asp925Gly
ENST00000460137.6:c.2556A>G	ENSP00000425003.1:n.2556A>G
ENST00000484238.6:n.1405A>G
NM_001193376.1:c.2774A>G	NP_001180305.1:p.Asp925Gly
NM_198253.2:c.2963A>G , LRG_343t1:c.2963A>G	NP_937983.2:p.Asp988Gly
XM_011514104.1:c.1433A>G	XP_011512406.1:p.Asp478Gly
XM_011514105.1:c.1319A>G	XP_011512407.1:p.Asp440Gly
XM_011514106.1:c.1319A>G	XP_011512408.1:p.Asp440Gly
NR_149162.1:n.2650A>G
NR_149163.1:n.2614A>G
NM_001193376.2:c.2774A>G	NP_001180305.1:p.Asp925Gly
NM_198253.3:c.2963A>G MANE Select	NP_937983.2:p.Asp988Gly
NR_149162.2:n.2671A>G
NR_149163.2:n.2635A>G
NM_001193376.3:c.2774A>G	NP_001180305.1:p.Asp925Gly
NR_149162.3:n.2671A>G
NR_149163.3:n.2635A>G