Canonical Allele Identifier: CA415186986

Gene: SSR4

Linked Data

• gnomAD v4: X-153798089-G-A
• MyVariant Identifiers: chrX:g.153063544G>A (hg19) ; chrX:g.153798089G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798089G>A , CM000685.2:g.153798089G>A	GRCh38
NC_000023.10:g.153063544G>A , CM000685.1:g.153063544G>A	GRCh37
NC_000023.9:g.152716738G>A	NCBI36
NG_041795.1:g.8915G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.370G>A MANE Select	ENSP00000359103.3:p.Asp124Asn
ENST00000320857.7:c.370G>A	ENSP00000317331.3:p.Asp124Asn
ENST00000370085.3:c.295G>A	ENSP00000359102.3:p.Asp99Asn
ENST00000370086.7:c.370G>A	ENSP00000359103.3:p.Asp124Asn
ENST00000370087.5:c.370G>A	ENSP00000359104.1:p.Asp124Asn
ENST00000447375.1:n.210G>A
ENST00000460616.5:n.2078G>A
ENST00000471880.5:n.573G>A
ENST00000482902.5:n.2197G>A
ENST00000485612.5:n.485G>A
ENST00000486204.5:n.442G>A
NM_001204526.1:c.403G>A	NP_001191455.1:p.Asp135Asn
NM_001204527.1:c.394G>A	NP_001191456.1:p.Asp132Asn
NM_006280.2:c.370G>A	NP_006271.1:p.Asp124Asn
NR_037927.1:n.715G>A
XM_011531186.1:c.370G>A	XP_011529488.1:p.Asp124Asn
XM_011531187.1:c.370G>A	XP_011529489.1:p.Asp124Asn
XM_017029756.1:c.181G>A	XP_016885245.1:p.Asp61Asn
XM_017029757.1:c.181G>A	XP_016885246.1:p.Asp61Asn
XM_024452428.1:c.181G>A	XP_024308196.1:p.Asp61Asn
NM_001204527.2:c.394G>A	NP_001191456.1:p.Asp132Asn
NM_006280.3:c.370G>A MANE Select	NP_006271.1:p.Asp124Asn