Canonical Allele Identifier: CA3185025

Gene: TERT

Linked Data

• ClinVar Variation Id: 1366402
• ClinVar RCV Id: RCV002406955 ; RCV002550983
• dbSNP Id: rs760727529
• ExAC: 5:1295028 G / A
• gnomAD v2: 5-1295028-G-A
• gnomAD v3: 5-1294913-G-A
• gnomAD v4: 5-1294913-G-A
• MyVariant Identifiers: chr5:g.1295028G>A (hg19) ; chr5:g.1294913G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1294913G>A , CM000667.2:g.1294913G>A	GRCh38
NC_000005.9:g.1295028G>A , CM000667.1:g.1295028G>A	GRCh37
NC_000005.8:g.1348028G>A	NCBI36
NG_009265.1:g.5135C>T , LRG_343:g.5135C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.77C>T MANE Select	ENSP00000309572.5:p.Thr26Met
ENST00000656021.1:c.77C>T	ENSP00000499759.1:p.Thr26Met
ENST00000310581.9:c.77C>T	ENSP00000309572.5:p.Thr26Met
ENST00000334602.10:c.77C>T	ENSP00000334346.6:p.Thr26Met
ENST00000460137.6:c.77C>T	ENSP00000425003.1:p.Thr26Met
ENST00000508104.2:c.77C>T	ENSP00000426042.2:p.Thr26Met
ENST00000522877.1:n.157C>T
NM_001193376.1:c.77C>T	NP_001180305.1:p.Thr26Met
NM_198253.2:c.77C>T , LRG_343t1:c.77C>T	NP_937983.2:p.Thr26Met
NR_149162.1:n.135C>T
NR_149163.1:n.135C>T
NM_001193376.2:c.77C>T	NP_001180305.1:p.Thr26Met
NM_198253.3:c.77C>T MANE Select	NP_937983.2:p.Thr26Met
NR_149162.2:n.156C>T
NR_149163.2:n.156C>T
NM_001193376.3:c.77C>T	NP_001180305.1:p.Thr26Met
NR_149162.3:n.156C>T
NR_149163.3:n.156C>T