Canonical Allele Identifier: CA2410564826

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913592G= , CM000684.2:g.49913592G=	GRCh38
NC_000022.10:g.50307240G= , CM000684.1:g.50307240G=	GRCh37
NC_000022.9:g.48693244G=	NCBI36
NG_008927.1:g.9867C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.162+12C= MANE Select	ENSP00000333813.5:n.162+12C=
ENST00000330817.10:c.162+12C=	ENSP00000333813.5:n.162+12C=
NM_024105.3:c.162+12C=	NP_077010.1:n.162+12C=
XM_011530369.1:c.162+12C=	XP_011528671.1:n.162+12C=
XM_011530370.1:c.162+12C=	XP_011528672.1:n.162+12C=
XM_011530371.1:c.162+12C=	XP_011528673.1:n.162+12C=
XM_011530371.2:c.162+12C=	XP_011528673.1:n.162+12C=
XM_017028936.1:c.162+12C=	XP_016884425.1:n.162+12C=
XM_017028937.1:c.162+12C=	XP_016884426.1:n.162+12C=
NM_024105.4:c.162+12C= MANE Select	NP_077010.1:n.162+12C=