Canonical Allele Identifier: CA2410564767

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913490C= , CM000684.2:g.49913490C=	GRCh38
NC_000022.10:g.50307138C= , CM000684.1:g.50307138C=	GRCh37
NC_000022.9:g.48693142C=	NCBI36
NG_008927.1:g.9969G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330817.11:c.190G= MANE Select	ENSP00000333813.5:p.Val64=
ENST00000330817.10:c.190G=	ENSP00000333813.5:p.Val64=
NM_024105.3:c.190G=	NP_077010.1:p.Val64=
XM_011530369.1:c.190G=	XP_011528671.1:p.Val64=
XM_011530370.1:c.190G=	XP_011528672.1:p.Val64=
XM_011530371.1:c.190G=	XP_011528673.1:p.Val64=
XM_011530371.2:c.190G=	XP_011528673.1:p.Val64=
XM_017028936.1:c.190G=	XP_016884425.1:p.Val64=
XM_017028937.1:c.190G=	XP_016884426.1:p.Val64=
NM_024105.4:c.190G= MANE Select	NP_077010.1:p.Val64=