Canonical Allele Identifier: CA2410562578

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49909251T= , CM000684.2:g.49909251T=	GRCh38
NC_000022.10:g.50302899T= , CM000684.1:g.50302899T=	GRCh37
NC_000022.9:g.48688903T=	NCBI36
NG_008927.1:g.14208A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.761A= MANE Select	ENSP00000333813.5:p.Asn254=
ENST00000330817.10:c.761A=	ENSP00000333813.5:p.Asn254=
ENST00000492791.1:c.292A=
NM_024105.3:c.761A=	NP_077010.1:p.Asn254=
XM_011530369.1:c.761A=	XP_011528671.1:p.Asn254=
XM_011530370.1:c.761A=	XP_011528672.1:p.Asn254=
XM_011530371.1:c.761A=	XP_011528673.1:p.Asn254=
XM_011530371.2:c.761A=	XP_011528673.1:p.Asn254=
XM_017028936.1:c.761A=	XP_016884425.1:p.Asn254=
XM_017028937.1:c.761A=	XP_016884426.1:p.Asn254=
NM_024105.4:c.761A= MANE Select	NP_077010.1:p.Asn254=