Canonical Allele Identifier: CA2687662367
Gene: TMEM70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.73976301del , CM000670.2:g.73976301del GRCh38
NC_000008.10:g.74888536del , CM000670.1:g.74888536del GRCh37
NC_000008.9:g.75051090del NCBI36
NG_016618.1:g.5160del

Transcript Alleles

HGVS Amino-acid change
ENST00000312184.6:c.20del MANE Select ENSP00000312599.5:p.Gly7AlafsTer?
ENST00000312184.5:c.20del ENSP00000312599.5:p.Gly7AlafsTer?
ENST00000416961.6:c.20del ENSP00000407695.2:p.Gly7AlafsTer?
ENST00000517439.1:c.20del ENSP00000429467.1:p.Gly7AlafsTer?
ENST00000517614.1:n.83del
ENST00000520167.5:n.317+340del
ENST00000523794.1:n.575-4del
NM_001040613.2:c.20del NP_001035703.1:p.Gly7AlafsTer?
NM_017866.5:c.20del NP_060336.3:p.Gly7AlafsTer?
NR_033334.1:n.160del
NM_017866.6:c.20del MANE Select NP_060336.3:p.Gly7AlafsTer?
NM_001040613.3:c.20del NP_001035703.1:p.Gly7AlafsTer?
NR_033334.2:n.107del