Canonical Allele Identifier: CA359056093

Gene: TERT

Linked Data

• dbSNP Id: rs1751180263
• MyVariant Identifiers: chr5:g.1294050C>T (hg19) ; chr5:g.1293935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293935C>T , CM000667.2:g.1293935C>T	GRCh38
NC_000005.9:g.1294050C>T , CM000667.1:g.1294050C>T	GRCh37
NC_000005.8:g.1347050C>T	NCBI36
NG_009265.1:g.6113G>A , LRG_343:g.6113G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.951G>A MANE Select	ENSP00000309572.5:p.Trp317Ter
ENST00000656021.1:c.951G>A	ENSP00000499759.1:p.Trp317Ter
ENST00000310581.9:c.951G>A	ENSP00000309572.5:p.Trp317Ter
ENST00000334602.10:c.951G>A	ENSP00000334346.6:p.Trp317Ter
ENST00000460137.6:c.951G>A	ENSP00000425003.1:p.Trp317Ter
ENST00000508104.2:c.951G>A	ENSP00000426042.2:p.Trp317Ter
NM_001193376.1:c.951G>A	NP_001180305.1:p.Trp317Ter
NM_198253.2:c.951G>A , LRG_343t1:c.951G>A	NP_937983.2:p.Trp317Ter
NR_149162.1:n.1009G>A
NR_149163.1:n.1009G>A
NM_001193376.2:c.951G>A	NP_001180305.1:p.Trp317Ter
NM_198253.3:c.951G>A MANE Select	NP_937983.2:p.Trp317Ter
NR_149162.2:n.1030G>A
NR_149163.2:n.1030G>A
NM_001193376.3:c.951G>A	NP_001180305.1:p.Trp317Ter
NR_149162.3:n.1030G>A
NR_149163.3:n.1030G>A