Canonical Allele Identifier: CA408948452
Gene: SPATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49906143A>C , CM000682.2:g.49906143A>C GRCh38
NC_000020.10:g.48522680A>C , CM000682.1:g.48522680A>C GRCh37
NC_000020.9:g.47956087A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.1039T>G MANE Select ENSP00000289431.5:p.Tyr347Asp
ENST00000289431.9:c.1039T>G ENSP00000289431.5:p.Tyr347Asp
ENST00000422556.1:c.1039T>G ENSP00000416799.1:p.Tyr347Asp
NM_001135773.1:c.1039T>G NP_001129245.1:p.Tyr347Asp
NM_006038.3:c.1039T>G NP_006029.1:p.Tyr347Asp
XM_006723894.1:c.1039T>G XP_006723957.1:p.Tyr347Asp
XM_011529116.1:c.1039T>G XP_011527418.1:p.Tyr347Asp
NM_006038.4:c.1039T>G MANE Select NP_006029.1:p.Tyr347Asp
NM_001135773.2:c.1039T>G NP_001129245.1:p.Tyr347Asp