Canonical Allele Identifier: CA2368281169
Gene: SPATA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905541A= , CM000682.2:g.49905541A= GRCh38
NC_000020.10:g.48522078A= , CM000682.1:g.48522078A= GRCh37
NC_000020.9:g.47955485A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.*78T= MANE Select ENSP00000289431.5:n.*78T=
ENST00000289431.9:c.*78T= ENSP00000289431.5:n.*78T=
ENST00000422556.1:c.*78T= ENSP00000416799.1:n.*78T=
NM_001135773.1:c.*78T= NP_001129245.1:n.*78T=
NM_006038.3:c.*78T= NP_006029.1:n.*78T=
XM_006723894.1:c.*78T= XP_006723957.1:n.*78T=
XM_011529116.1:c.*78T= XP_011527418.1:n.*78T=
NM_006038.4:c.*78T= MANE Select NP_006029.1:n.*78T=
NM_001135773.2:c.*78T= NP_001129245.1:n.*78T=
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