Canonical Allele Identifier: CA359069858

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1260629A>T (hg19) ; chr5:g.1260514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260514A>T , CM000667.2:g.1260514A>T	GRCh38
NC_000005.9:g.1260629A>T , CM000667.1:g.1260629A>T	GRCh37
NC_000005.8:g.1313629A>T	NCBI36
NG_009265.1:g.39534T>A , LRG_343:g.39534T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2930T>A MANE Select	ENSP00000309572.5:p.Val977Asp
ENST00000656021.1:c.*2476T>A	ENSP00000499759.1:n.*2476T>A
ENST00000667927.1:n.218T>A
ENST00000310581.9:c.2930T>A	ENSP00000309572.5:p.Val977Asp
ENST00000334602.10:c.2741T>A	ENSP00000334346.6:p.Val914Asp
ENST00000460137.6:c.2523T>A	ENSP00000425003.1:n.2523T>A
ENST00000484238.6:n.1372T>A
NM_001193376.1:c.2741T>A	NP_001180305.1:p.Val914Asp
NM_198253.2:c.2930T>A , LRG_343t1:c.2930T>A	NP_937983.2:p.Val977Asp
XM_011514104.1:c.1400T>A	XP_011512406.1:p.Val467Asp
XM_011514105.1:c.1286T>A	XP_011512407.1:p.Val429Asp
XM_011514106.1:c.1286T>A	XP_011512408.1:p.Val429Asp
NR_149162.1:n.2617T>A
NR_149163.1:n.2581T>A
NM_001193376.2:c.2741T>A	NP_001180305.1:p.Val914Asp
NM_198253.3:c.2930T>A MANE Select	NP_937983.2:p.Val977Asp
NR_149162.2:n.2638T>A
NR_149163.2:n.2602T>A
NM_001193376.3:c.2741T>A	NP_001180305.1:p.Val914Asp
NR_149162.3:n.2638T>A
NR_149163.3:n.2602T>A