Canonical Allele Identifier: CA2078984340
Gene: SPATA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24084217G= , CM000675.2:g.24084217G= GRCh38
NC_000013.10:g.24658356G= , CM000675.1:g.24658356G= GRCh37
NC_000013.9:g.23556356G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382141.4:c.-112+66516G= ENSP00000371576.4:n.-112+66516G=
ENST00000424834.6:c.-112+66516G= ENSP00000398560.2:n.-112+66516G=
NM_001286792.1:c.75+66516G= NP_001273721.1:n.75+66516G=
NM_001286792.2:c.75+66516G= NP_001273721.1:n.75+66516G=