Canonical Allele Identifier: CA2368281189
Gene: SPATA2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905560C= , CM000682.2:g.49905560C= GRCh38
NC_000020.10:g.48522097C= , CM000682.1:g.48522097C= GRCh37
NC_000020.9:g.47955504C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.*59G= MANE Select ENSP00000289431.5:n.*59G=
ENST00000289431.9:c.*59G= ENSP00000289431.5:n.*59G=
ENST00000422556.1:c.*59G= ENSP00000416799.1:n.*59G=
NM_001135773.1:c.*59G= NP_001129245.1:n.*59G=
NM_006038.3:c.*59G= NP_006029.1:n.*59G=
XM_006723894.1:c.*59G= XP_006723957.1:n.*59G=
XM_011529116.1:c.*59G= XP_011527418.1:n.*59G=
NM_006038.4:c.*59G= MANE Select NP_006029.1:n.*59G=
NM_001135773.2:c.*59G= NP_001129245.1:n.*59G=
Search 100 bp 5'
Search 100 bp 3'