Canonical Allele Identifier: CA415187032

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063563C>A (hg19) ; chrX:g.153798108C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798108C>A , CM000685.2:g.153798108C>A	GRCh38
NC_000023.10:g.153063563C>A , CM000685.1:g.153063563C>A	GRCh37
NC_000023.9:g.152716757C>A	NCBI36
NG_041795.1:g.8934C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.389C>A MANE Select	ENSP00000359103.3:p.Pro130His
ENST00000320857.7:c.389C>A	ENSP00000317331.3:p.Pro130His
ENST00000370085.3:c.314C>A	ENSP00000359102.3:p.Pro105His
ENST00000370086.7:c.389C>A	ENSP00000359103.3:p.Pro130His
ENST00000370087.5:c.389C>A	ENSP00000359104.1:p.Pro130His
ENST00000447375.1:n.229C>A
ENST00000460616.5:n.2097C>A
ENST00000471880.5:n.592C>A
ENST00000482902.5:n.2216C>A
ENST00000485612.5:n.504C>A
ENST00000486204.5:n.461C>A
NM_001204526.1:c.422C>A	NP_001191455.1:p.Pro141His
NM_001204527.1:c.413C>A	NP_001191456.1:p.Pro138His
NM_006280.2:c.389C>A	NP_006271.1:p.Pro130His
NR_037927.1:n.734C>A
XM_011531186.1:c.389C>A	XP_011529488.1:p.Pro130His
XM_011531187.1:c.389C>A	XP_011529489.1:p.Pro130His
XM_017029756.1:c.200C>A	XP_016885245.1:p.Pro67His
XM_017029757.1:c.200C>A	XP_016885246.1:p.Pro67His
XM_024452428.1:c.200C>A	XP_024308196.1:p.Pro67His
NM_001204527.2:c.413C>A	NP_001191456.1:p.Pro138His
NM_006280.3:c.389C>A MANE Select	NP_006271.1:p.Pro130His