Canonical Allele Identifier: CA2078984282
Gene: SPATA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24084121T= , CM000675.2:g.24084121T= GRCh38
NC_000013.10:g.24658260T= , CM000675.1:g.24658260T= GRCh37
NC_000013.9:g.23556260T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382141.4:c.-112+66420T= ENSP00000371576.4:n.-112+66420T=
ENST00000424834.6:c.-112+66420T= ENSP00000398560.2:n.-112+66420T=
NM_001286792.1:c.75+66420T= NP_001273721.1:n.75+66420T=
NM_001286792.2:c.75+66420T= NP_001273721.1:n.75+66420T=