Canonical Allele Identifier: CA415186975

Gene: SSR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.365A>C MANE Select	ENSP00000359103.3:p.Asn122Thr
ENST00000320857.7:c.365A>C	ENSP00000317331.3:p.Asn122Thr
ENST00000370085.3:c.290A>C	ENSP00000359102.3:p.Asn97Thr
ENST00000370086.7:c.365A>C	ENSP00000359103.3:p.Asn122Thr
ENST00000370087.5:c.365A>C	ENSP00000359104.1:p.Asn122Thr
ENST00000447375.1:n.205A>C
ENST00000460616.5:n.2073A>C
ENST00000471880.5:n.568A>C
ENST00000482902.5:n.2192A>C
ENST00000485612.5:n.480A>C
ENST00000486204.5:n.437A>C
NM_001204526.1:c.398A>C	NP_001191455.1:p.Asn133Thr
NM_001204527.1:c.389A>C	NP_001191456.1:p.Asn130Thr
NM_006280.2:c.365A>C	NP_006271.1:p.Asn122Thr
NR_037927.1:n.710A>C
XM_011531186.1:c.365A>C	XP_011529488.1:p.Asn122Thr
XM_011531187.1:c.365A>C	XP_011529489.1:p.Asn122Thr
XM_017029756.1:c.176A>C	XP_016885245.1:p.Asn59Thr
XM_017029757.1:c.176A>C	XP_016885246.1:p.Asn59Thr
XM_024452428.1:c.176A>C	XP_024308196.1:p.Asn59Thr
NM_001204527.2:c.389A>C	NP_001191456.1:p.Asn130Thr
NM_006280.3:c.365A>C MANE Select	NP_006271.1:p.Asn122Thr