Canonical Allele Identifier: CA415187109

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063585C>A (hg19) ; chrX:g.153798130C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798130C>A , CM000685.2:g.153798130C>A	GRCh38
NC_000023.10:g.153063585C>A , CM000685.1:g.153063585C>A	GRCh37
NC_000023.9:g.152716779C>A	NCBI36
NG_041795.1:g.8956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.411C>A MANE Select	ENSP00000359103.3:p.Asp137Glu
ENST00000320857.7:c.411C>A	ENSP00000317331.3:p.Asp137Glu
ENST00000370085.3:c.336C>A	ENSP00000359102.3:p.Asp112Glu
ENST00000370086.7:c.411C>A	ENSP00000359103.3:p.Asp137Glu
ENST00000370087.5:c.411C>A	ENSP00000359104.1:p.Asp137Glu
ENST00000447375.1:n.251C>A
ENST00000460616.5:n.2119C>A
ENST00000471880.5:n.614C>A
ENST00000482902.5:n.2238C>A
ENST00000485612.5:n.526C>A
ENST00000486204.5:n.483C>A
NM_001204526.1:c.444C>A	NP_001191455.1:p.Asp148Glu
NM_001204527.1:c.435C>A	NP_001191456.1:p.Asp145Glu
NM_006280.2:c.411C>A	NP_006271.1:p.Asp137Glu
NR_037927.1:n.756C>A
XM_011531186.1:c.411C>A	XP_011529488.1:p.Asp137Glu
XM_011531187.1:c.411C>A	XP_011529489.1:p.Asp137Glu
XM_017029756.1:c.222C>A	XP_016885245.1:p.Asp74Glu
XM_017029757.1:c.222C>A	XP_016885246.1:p.Asp74Glu
XM_024452428.1:c.222C>A	XP_024308196.1:p.Asp74Glu
NM_001204527.2:c.435C>A	NP_001191456.1:p.Asp145Glu
NM_006280.3:c.411C>A MANE Select	NP_006271.1:p.Asp137Glu