Canonical Allele Identifier: CA359073205

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1266610G>A (hg19) ; chr5:g.1266495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266495G>A , CM000667.2:g.1266495G>A	GRCh38
NC_000005.9:g.1266610G>A , CM000667.1:g.1266610G>A	GRCh37
NC_000005.8:g.1319610G>A	NCBI36
NG_009265.1:g.33553C>T , LRG_343:g.33553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2623C>T MANE Select	ENSP00000309572.5:p.Pro875Ser
ENST00000656021.1:c.*2169C>T	ENSP00000499759.1:n.*2169C>T
ENST00000310581.9:c.2623C>T	ENSP00000309572.5:p.Pro875Ser
ENST00000334602.10:c.2623C>T	ENSP00000334346.6:p.Pro875Ser
ENST00000460137.6:c.2405C>T	ENSP00000425003.1:n.2405C>T
ENST00000484238.6:n.1254C>T
ENST00000503656.1:n.30C>T
ENST00000508104.2:c.2441C>T	ENSP00000426042.2:n.2441C>T
NM_001193376.1:c.2623C>T	NP_001180305.1:p.Pro875Ser
NM_198253.2:c.2623C>T , LRG_343t1:c.2623C>T	NP_937983.2:p.Pro875Ser
XM_011514104.1:c.1093C>T	XP_011512406.1:p.Pro365Ser
XM_011514105.1:c.979C>T	XP_011512407.1:p.Pro327Ser
XM_011514106.1:c.979C>T	XP_011512408.1:p.Pro327Ser
NR_149162.1:n.2499C>T
NR_149163.1:n.2463C>T
NM_001193376.2:c.2623C>T	NP_001180305.1:p.Pro875Ser
NM_198253.3:c.2623C>T MANE Select	NP_937983.2:p.Pro875Ser
NR_149162.2:n.2520C>T
NR_149163.2:n.2484C>T
NM_001193376.3:c.2623C>T	NP_001180305.1:p.Pro875Ser
NR_149162.3:n.2520C>T
NR_149163.3:n.2484C>T