Canonical Allele Identifier: CA2466480554

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798074_153798076delinsCAG , CM000685.2:g.153798074_153798076delinsCAG	GRCh38
NC_000023.10:g.153063529_153063531delinsCAG , CM000685.1:g.153063529_153063531delinsCAG	GRCh37
NC_000023.9:g.152716723_152716725delinsCAG	NCBI36
NG_041795.1:g.8900_8902delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.355_357delinsCAG MANE Select	ENSP00000359103.3:p.Gln119=
ENST00000320857.7:c.355_357delinsCAG	ENSP00000317331.3:p.Gln119=
ENST00000370085.3:c.280_282delinsCAG	ENSP00000359102.3:p.Gln94=
ENST00000370086.7:c.355_357delinsCAG	ENSP00000359103.3:p.Gln119=
ENST00000370087.5:c.355_357delinsCAG	ENSP00000359104.1:p.Gln119=
ENST00000447375.1:n.195_197delinsCAG
ENST00000460616.5:n.2063_2065delinsCAG
ENST00000471880.5:n.558_560delinsCAG
ENST00000482902.5:n.2182_2184delinsCAG
ENST00000485612.5:n.470_472delinsCAG
ENST00000486204.5:n.427_429delinsCAG
NM_001204526.1:c.388_390delinsCAG	NP_001191455.1:p.Gln130=
NM_001204527.1:c.379_381delinsCAG	NP_001191456.1:p.Gln127=
NM_006280.2:c.355_357delinsCAG	NP_006271.1:p.Gln119=
NR_037927.1:n.700_702delinsCAG
XM_011531186.1:c.355_357delinsCAG	XP_011529488.1:p.Gln119=
XM_011531187.1:c.355_357delinsCAG	XP_011529489.1:p.Gln119=
XM_017029756.1:c.166_168delinsCAG	XP_016885245.1:p.Gln56=
XM_017029757.1:c.166_168delinsCAG	XP_016885246.1:p.Gln56=
XM_024452428.1:c.166_168delinsCAG	XP_024308196.1:p.Gln56=
NM_001204527.2:c.379_381delinsCAG	NP_001191456.1:p.Gln127=
NM_006280.3:c.355_357delinsCAG MANE Select	NP_006271.1:p.Gln119=