Canonical Allele Identifier: CA2466480559

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798085C= , CM000685.2:g.153798085C=	GRCh38
NC_000023.10:g.153063540C= , CM000685.1:g.153063540C=	GRCh37
NC_000023.9:g.152716734C=	NCBI36
NG_041795.1:g.8911C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.366C= MANE Select	ENSP00000359103.3:p.Asn122=
ENST00000320857.7:c.366C=	ENSP00000317331.3:p.Asn122=
ENST00000370085.3:c.291C=	ENSP00000359102.3:p.Asn97=
ENST00000370086.7:c.366C=	ENSP00000359103.3:p.Asn122=
ENST00000370087.5:c.366C=	ENSP00000359104.1:p.Asn122=
ENST00000447375.1:n.206C=
ENST00000460616.5:n.2074C=
ENST00000471880.5:n.569C=
ENST00000482902.5:n.2193C=
ENST00000485612.5:n.481C=
ENST00000486204.5:n.438C=
NM_001204526.1:c.399C=	NP_001191455.1:p.Asn133=
NM_001204527.1:c.390C=	NP_001191456.1:p.Asn130=
NM_006280.2:c.366C=	NP_006271.1:p.Asn122=
NR_037927.1:n.711C=
XM_011531186.1:c.366C=	XP_011529488.1:p.Asn122=
XM_011531187.1:c.366C=	XP_011529489.1:p.Asn122=
XM_017029756.1:c.177C=	XP_016885245.1:p.Asn59=
XM_017029757.1:c.177C=	XP_016885246.1:p.Asn59=
XM_024452428.1:c.177C=	XP_024308196.1:p.Asn59=
NM_001204527.2:c.390C=	NP_001191456.1:p.Asn130=
NM_006280.3:c.366C= MANE Select	NP_006271.1:p.Asn122=