Canonical Allele Identifier: CA359069927

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1260639G>T (hg19) ; chr5:g.1260524G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260524G>T , CM000667.2:g.1260524G>T	GRCh38
NC_000005.9:g.1260639G>T , CM000667.1:g.1260639G>T	GRCh37
NC_000005.8:g.1313639G>T	NCBI36
NG_009265.1:g.39524C>A , LRG_343:g.39524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2920C>A MANE Select	ENSP00000309572.5:p.Leu974Ile
ENST00000656021.1:c.*2466C>A	ENSP00000499759.1:n.*2466C>A
ENST00000667927.1:n.208C>A
ENST00000310581.9:c.2920C>A	ENSP00000309572.5:p.Leu974Ile
ENST00000334602.10:c.2731C>A	ENSP00000334346.6:p.Leu911Ile
ENST00000460137.6:c.2513C>A	ENSP00000425003.1:n.2513C>A
ENST00000484238.6:n.1362C>A
NM_001193376.1:c.2731C>A	NP_001180305.1:p.Leu911Ile
NM_198253.2:c.2920C>A , LRG_343t1:c.2920C>A	NP_937983.2:p.Leu974Ile
XM_011514104.1:c.1390C>A	XP_011512406.1:p.Leu464Ile
XM_011514105.1:c.1276C>A	XP_011512407.1:p.Leu426Ile
XM_011514106.1:c.1276C>A	XP_011512408.1:p.Leu426Ile
NR_149162.1:n.2607C>A
NR_149163.1:n.2571C>A
NM_001193376.2:c.2731C>A	NP_001180305.1:p.Leu911Ile
NM_198253.3:c.2920C>A MANE Select	NP_937983.2:p.Leu974Ile
NR_149162.2:n.2628C>A
NR_149163.2:n.2592C>A
NM_001193376.3:c.2731C>A	NP_001180305.1:p.Leu911Ile
NR_149162.3:n.2628C>A
NR_149163.3:n.2592C>A