Canonical Allele Identifier: CA415186976

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063539A>G (hg19) ; chrX:g.153798084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798084A>G , CM000685.2:g.153798084A>G	GRCh38
NC_000023.10:g.153063539A>G , CM000685.1:g.153063539A>G	GRCh37
NC_000023.9:g.152716733A>G	NCBI36
NG_041795.1:g.8910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.365A>G MANE Select	ENSP00000359103.3:p.Asn122Ser
ENST00000320857.7:c.365A>G	ENSP00000317331.3:p.Asn122Ser
ENST00000370085.3:c.290A>G	ENSP00000359102.3:p.Asn97Ser
ENST00000370086.7:c.365A>G	ENSP00000359103.3:p.Asn122Ser
ENST00000370087.5:c.365A>G	ENSP00000359104.1:p.Asn122Ser
ENST00000447375.1:n.205A>G
ENST00000460616.5:n.2073A>G
ENST00000471880.5:n.568A>G
ENST00000482902.5:n.2192A>G
ENST00000485612.5:n.480A>G
ENST00000486204.5:n.437A>G
NM_001204526.1:c.398A>G	NP_001191455.1:p.Asn133Ser
NM_001204527.1:c.389A>G	NP_001191456.1:p.Asn130Ser
NM_006280.2:c.365A>G	NP_006271.1:p.Asn122Ser
NR_037927.1:n.710A>G
XM_011531186.1:c.365A>G	XP_011529488.1:p.Asn122Ser
XM_011531187.1:c.365A>G	XP_011529489.1:p.Asn122Ser
XM_017029756.1:c.176A>G	XP_016885245.1:p.Asn59Ser
XM_017029757.1:c.176A>G	XP_016885246.1:p.Asn59Ser
XM_024452428.1:c.176A>G	XP_024308196.1:p.Asn59Ser
NM_001204527.2:c.389A>G	NP_001191456.1:p.Asn130Ser
NM_006280.3:c.365A>G MANE Select	NP_006271.1:p.Asn122Ser