Canonical Allele Identifier: CA2368281172

Gene: SPATA2

Linked Data

• dbSNP Id: rs943092531

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49905544C>G , CM000682.2:g.49905544C>G	GRCh38
NC_000020.10:g.48522081C>G , CM000682.1:g.48522081C>G	GRCh37
NC_000020.9:g.47955488C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.*75G>C MANE Select	ENSP00000289431.5:n.*75G>C
ENST00000289431.9:c.*75G>C	ENSP00000289431.5:n.*75G>C
ENST00000422556.1:c.*75G>C	ENSP00000416799.1:n.*75G>C
NM_001135773.1:c.*75G>C	NP_001129245.1:n.*75G>C
NM_006038.3:c.*75G>C	NP_006029.1:n.*75G>C
XM_006723894.1:c.*75G>C	XP_006723957.1:n.*75G>C
XM_011529116.1:c.*75G>C	XP_011527418.1:n.*75G>C
NM_006038.4:c.*75G>C MANE Select	NP_006029.1:n.*75G>C
NM_001135773.2:c.*75G>C	NP_001129245.1:n.*75G>C