Canonical Allele Identifier: CA2368281449
Gene: SPATA2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49906125G= , CM000682.2:g.49906125G= GRCh38
NC_000020.10:g.48522662G= , CM000682.1:g.48522662G= GRCh37
NC_000020.9:g.47956069G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.1057C= MANE Select ENSP00000289431.5:p.Leu353=
ENST00000289431.9:c.1057C= ENSP00000289431.5:p.Leu353=
ENST00000422556.1:c.1057C= ENSP00000416799.1:p.Leu353=
NM_001135773.1:c.1057C= NP_001129245.1:p.Leu353=
NM_006038.3:c.1057C= NP_006029.1:p.Leu353=
XM_006723894.1:c.1057C= XP_006723957.1:p.Leu353=
XM_011529116.1:c.1057C= XP_011527418.1:p.Leu353=
NM_006038.4:c.1057C= MANE Select NP_006029.1:p.Leu353=
NM_001135773.2:c.1057C= NP_001129245.1:p.Leu353=
Search 100 bp 5'
Search 100 bp 3'