Canonical Allele Identifier: CA2368281208
Gene: SPATA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905581T= , CM000682.2:g.49905581T= GRCh38
NC_000020.10:g.48522118T= , CM000682.1:g.48522118T= GRCh37
NC_000020.9:g.47955525T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.*38A= MANE Select ENSP00000289431.5:n.*38A=
ENST00000289431.9:c.*38A= ENSP00000289431.5:n.*38A=
ENST00000422556.1:c.*38A= ENSP00000416799.1:n.*38A=
NM_001135773.1:c.*38A= NP_001129245.1:n.*38A=
NM_006038.3:c.*38A= NP_006029.1:n.*38A=
XM_006723894.1:c.*38A= XP_006723957.1:n.*38A=
XM_011529116.1:c.*38A= XP_011527418.1:n.*38A=
NM_006038.4:c.*38A= MANE Select NP_006029.1:n.*38A=
NM_001135773.2:c.*38A= NP_001129245.1:n.*38A=
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