Canonical Allele Identifier: CA2368281182
Gene: SPATA2 HGNC NCBI

Linked Data

dbSNP Id: rs2090135261
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905554T>G , CM000682.2:g.49905554T>G GRCh38
NC_000020.10:g.48522091T>G , CM000682.1:g.48522091T>G GRCh37
NC_000020.9:g.47955498T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.*65A>C MANE Select ENSP00000289431.5:n.*65A>C
ENST00000289431.9:c.*65A>C ENSP00000289431.5:n.*65A>C
ENST00000422556.1:c.*65A>C ENSP00000416799.1:n.*65A>C
NM_001135773.1:c.*65A>C NP_001129245.1:n.*65A>C
NM_006038.3:c.*65A>C NP_006029.1:n.*65A>C
XM_006723894.1:c.*65A>C XP_006723957.1:n.*65A>C
XM_011529116.1:c.*65A>C XP_011527418.1:n.*65A>C
NM_006038.4:c.*65A>C MANE Select NP_006029.1:n.*65A>C
NM_001135773.2:c.*65A>C NP_001129245.1:n.*65A>C
Search 100 bp 5'
Search 100 bp 3'