Canonical Allele Identifier: CA514983530

Gene: ALG12

Linked Data

• MyVariant Identifiers: chr22:g.50302892C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49909244C>G , CM000684.2:g.49909244C>G	GRCh38
NC_000022.10:g.50302892C>G , CM000684.1:g.50302892C>G	GRCh37
NC_000022.9:g.48688896C>G	NCBI36
NG_008927.1:g.14215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.768G>C MANE Select	ENSP00000333813.5:p.Gly256=
ENST00000330817.10:c.768G>C	ENSP00000333813.5:p.Gly256=
ENST00000492791.1:c.299G>C
NM_024105.3:c.768G>C	NP_077010.1:p.Gly256=
XM_011530369.1:c.768G>C	XP_011528671.1:p.Gly256=
XM_011530370.1:c.768G>C	XP_011528672.1:p.Gly256=
XM_011530371.1:c.768G>C	XP_011528673.1:p.Gly256=
XM_011530371.2:c.768G>C	XP_011528673.1:p.Gly256=
XM_017028936.1:c.768G>C	XP_016884425.1:p.Gly256=
XM_017028937.1:c.768G>C	XP_016884426.1:p.Gly256=
NM_024105.4:c.768G>C MANE Select	NP_077010.1:p.Gly256=