Canonical Allele Identifier: CA359073198

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1266609G>A (hg19) ; chr5:g.1266494G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266494G>A , CM000667.2:g.1266494G>A	GRCh38
NC_000005.9:g.1266609G>A , CM000667.1:g.1266609G>A	GRCh37
NC_000005.8:g.1319609G>A	NCBI36
NG_009265.1:g.33554C>T , LRG_343:g.33554C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2624C>T MANE Select	ENSP00000309572.5:p.Pro875Leu
ENST00000656021.1:c.*2170C>T	ENSP00000499759.1:n.*2170C>T
ENST00000310581.9:c.2624C>T	ENSP00000309572.5:p.Pro875Leu
ENST00000334602.10:c.2624C>T	ENSP00000334346.6:p.Pro875Leu
ENST00000460137.6:c.2406C>T	ENSP00000425003.1:n.2406C>T
ENST00000484238.6:n.1255C>T
ENST00000503656.1:n.31C>T
ENST00000508104.2:c.2442C>T	ENSP00000426042.2:n.2442C>T
NM_001193376.1:c.2624C>T	NP_001180305.1:p.Pro875Leu
NM_198253.2:c.2624C>T , LRG_343t1:c.2624C>T	NP_937983.2:p.Pro875Leu
XM_011514104.1:c.1094C>T	XP_011512406.1:p.Pro365Leu
XM_011514105.1:c.980C>T	XP_011512407.1:p.Pro327Leu
XM_011514106.1:c.980C>T	XP_011512408.1:p.Pro327Leu
NR_149162.1:n.2500C>T
NR_149163.1:n.2464C>T
NM_001193376.2:c.2624C>T	NP_001180305.1:p.Pro875Leu
NM_198253.3:c.2624C>T MANE Select	NP_937983.2:p.Pro875Leu
NR_149162.2:n.2521C>T
NR_149163.2:n.2485C>T
NM_001193376.3:c.2624C>T	NP_001180305.1:p.Pro875Leu
NR_149162.3:n.2521C>T
NR_149163.3:n.2485C>T