Canonical Allele Identifier: CA2466480555

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798076G= , CM000685.2:g.153798076G=	GRCh38
NC_000023.10:g.153063531G= , CM000685.1:g.153063531G=	GRCh37
NC_000023.9:g.152716725G=	NCBI36
NG_041795.1:g.8902G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.357G= MANE Select	ENSP00000359103.3:p.Gln119=
ENST00000320857.7:c.357G=	ENSP00000317331.3:p.Gln119=
ENST00000370085.3:c.282G=	ENSP00000359102.3:p.Gln94=
ENST00000370086.7:c.357G=	ENSP00000359103.3:p.Gln119=
ENST00000370087.5:c.357G=	ENSP00000359104.1:p.Gln119=
ENST00000447375.1:n.197G=
ENST00000460616.5:n.2065G=
ENST00000471880.5:n.560G=
ENST00000482902.5:n.2184G=
ENST00000485612.5:n.472G=
ENST00000486204.5:n.429G=
NM_001204526.1:c.390G=	NP_001191455.1:p.Gln130=
NM_001204527.1:c.381G=	NP_001191456.1:p.Gln127=
NM_006280.2:c.357G=	NP_006271.1:p.Gln119=
NR_037927.1:n.702G=
XM_011531186.1:c.357G=	XP_011529488.1:p.Gln119=
XM_011531187.1:c.357G=	XP_011529489.1:p.Gln119=
XM_017029756.1:c.168G=	XP_016885245.1:p.Gln56=
XM_017029757.1:c.168G=	XP_016885246.1:p.Gln56=
XM_024452428.1:c.168G=	XP_024308196.1:p.Gln56=
NM_001204527.2:c.381G=	NP_001191456.1:p.Gln127=
NM_006280.3:c.357G= MANE Select	NP_006271.1:p.Gln119=