Canonical Allele Identifier: CA2417074350

Gene: AP1S2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15852346C= , CM000685.2:g.15852346C=	GRCh38
NC_000023.10:g.15870469C= , CM000685.1:g.15870469C=	GRCh37
NC_000023.9:g.15780390C=	NCBI36
NG_009274.1:g.7632G=
NG_009274.2:g.7632G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450644.2:c.179G=	ENSP00000389474.2:p.Arg60=
ENST00000479184.2:c.179G=	ENSP00000500850.1:p.Arg60=
ENST00000545766.7:c.47G=	ENSP00000444957.3:p.Arg16=
ENST00000671830.1:c.179G=	ENSP00000500483.1:p.Arg60=
ENST00000672063.1:c.179G=	ENSP00000500737.1:p.Arg60=
ENST00000672987.1:c.179G= MANE Select	ENSP00000500695.1:p.Arg60=
ENST00000673445.1:c.179G=	ENSP00000500798.1:p.Arg60=
ENST00000673591.1:c.179G=	ENSP00000500066.1:p.Arg60=
ENST00000329235.6:c.179G=	ENSP00000328789.2:p.Arg60=
ENST00000380291.5:c.179G=	ENSP00000369645.1:p.Arg60=
ENST00000450644.1:c.157G=
ENST00000452376.5:c.168G=
ENST00000545766.5:c.179G=	ENSP00000444957.2:p.Arg60=
NM_001272071.1:c.179G=	NP_001259000.1:p.Arg60=
NM_003916.4:c.179G=	NP_003907.3:p.Arg60=
XM_005274614.3:c.305G=	XP_005274671.1:p.Arg102=
XM_011545599.1:c.305G=	XP_011543901.1:p.Arg102=
XR_247289.2:n.458G=
XR_247290.3:n.393G=
XM_017029925.1:c.305G=	XP_016885414.1:p.Arg102=
XM_017029926.2:c.305G=	XP_016885415.1:p.Arg102=
XR_001755741.2:n.458G=
XR_002958809.1:n.229G=
XR_247289.3:n.458G=
XR_247290.4:n.458G=
NM_001272071.2:c.179G= MANE Select	NP_001259000.1:p.Arg60=
NM_001368994.1:c.179G=	NP_001355923.1:p.Arg60=
NM_001369007.1:c.179G=	NP_001355936.1:p.Arg60=
NM_001369008.1:c.179G=	NP_001355937.1:p.Arg60=
NM_003916.5:c.179G=	NP_003907.3:p.Arg60=
NR_160932.1:n.305G=
NR_160933.1:n.305G=