Canonical Allele Identifier: CA2368281221
Gene: SPATA2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905607G= , CM000682.2:g.49905607G= GRCh38
NC_000020.10:g.48522144G= , CM000682.1:g.48522144G= GRCh37
NC_000020.9:g.47955551G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.*12C= MANE Select ENSP00000289431.5:n.*12C=
ENST00000289431.9:c.*12C= ENSP00000289431.5:n.*12C=
ENST00000422556.1:c.*12C= ENSP00000416799.1:n.*12C=
NM_001135773.1:c.*12C= NP_001129245.1:n.*12C=
NM_006038.3:c.*12C= NP_006029.1:n.*12C=
XM_006723894.1:c.*12C= XP_006723957.1:n.*12C=
XM_011529116.1:c.*12C= XP_011527418.1:n.*12C=
NM_006038.4:c.*12C= MANE Select NP_006029.1:n.*12C=
NM_001135773.2:c.*12C= NP_001129245.1:n.*12C=
Search 100 bp 5'
Search 100 bp 3'