Canonical Allele Identifier: CA180365307
Gene: TPD52 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1042638

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80037711G>A , CM000670.2:g.80037711G>A GRCh38
NC_000008.10:g.80949946G>A , CM000670.1:g.80949946G>A GRCh37
NC_000008.9:g.81112501G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001025252.2:c.*405C>T VV NP_001020423.1:p.=
NM_001025253.2:c.*405C>T VV NP_001020424.1:p.=
NM_001287140.1:c.*405C>T VV NP_001274069.1:p.=
NM_001287142.1:c.*405C>T VV NP_001274071.1:p.=
NM_001287143.1:c.*405C>T VV NP_001274072.1:p.=
NM_001287144.1:c.*515C>T VV NP_001274073.1:p.=
NM_005079.3:c.*405C>T VV NP_005070.1:p.=
NR_105033.1:n.1597C>T
NR_105034.1:n.1060C>T
NR_105035.1:n.1246C>T
NR_105036.1:n.1190C>T
NR_105037.1:n.1191C>T
ENST00000379096.9:c.*405C>T ENSP00000368390.4:p.=
ENST00000379097.7:c.*405C>T ENSP00000368391.3:p.=
ENST00000448733.3:c.*405C>T ENSP00000410222.2:p.=
ENST00000517427.5:c.*405C>T ENSP00000429351.1:p.=
ENST00000517462.6:c.*763C>T ENSP00000429708.1:p.=
ENST00000518937.5:c.*405C>T ENSP00000429915.1:p.=
ENST00000519303.6:c.*405C>T ENSP00000428951.1:p.=
ENST00000520527.5:c.*405C>T ENSP00000429309.1:p.=
ENST00000522938.5:c.555+4909C>T ENSP00000430858.2:p.=
ENST00000523395.5:n.739C>T