Canonical Allele Identifier: CA1796855320
Community Standard Title: NC_000008.11:g.80183160C=
Gene: TPD52 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80183160C= , CM000670.2:g.80183160C= GRCh38
NC_000008.10:g.81095395C= , CM000670.1:g.81095395C= GRCh37
NC_000008.9:g.81257950C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000519250.5:n.235+35309G=
ENST00000520035.5:n.176-4881G=
ENST00000523564.2:n.63-22G=
ENST00000602950.1:n.223-22G=
XR_929092.1:n.557-22G=
XR_929092.2:n.590-22G=
XR_929093.1:n.557-22G=
XR_929093.2:n.590-22G=
XR_929095.1:n.557-22G=
XR_929095.2:n.591-22G=