Canonical Allele Identifier: CA2842486016

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913550G>T , CM000684.2:g.49913550G>T	GRCh38
NC_000022.10:g.50307198G>T , CM000684.1:g.50307198G>T	GRCh37
NC_000022.9:g.48693202G>T	NCBI36
NG_008927.1:g.9909C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.163-33C>A MANE Select	ENSP00000333813.5:n.163-33C>A
ENST00000330817.10:c.163-33C>A	ENSP00000333813.5:n.163-33C>A
NM_024105.3:c.163-33C>A	NP_077010.1:n.163-33C>A
XM_011530369.1:c.163-33C>A	XP_011528671.1:n.163-33C>A
XM_011530370.1:c.163-33C>A	XP_011528672.1:n.163-33C>A
XM_011530371.1:c.163-33C>A	XP_011528673.1:n.163-33C>A
XM_011530371.2:c.163-33C>A	XP_011528673.1:n.163-33C>A
XM_017028936.1:c.163-33C>A	XP_016884425.1:n.163-33C>A
XM_017028937.1:c.163-33C>A	XP_016884426.1:n.163-33C>A
NM_024105.4:c.163-33C>A MANE Select	NP_077010.1:n.163-33C>A