Canonical Allele Identifier: CA855731746
Gene: TPD52 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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