Canonical Allele Identifier: CA412081554

Gene: ALG12

Linked Data

• MyVariant Identifiers: chr22:g.50307350T>C (hg19) ; chr22:g.49913702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913702T>C , CM000684.2:g.49913702T>C	GRCh38
NC_000022.10:g.50307350T>C , CM000684.1:g.50307350T>C	GRCh37
NC_000022.9:g.48693354T>C	NCBI36
NG_008927.1:g.9757A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.64A>G MANE Select	ENSP00000333813.5:p.Thr22Ala
ENST00000330817.10:c.64A>G	ENSP00000333813.5:p.Thr22Ala
NM_024105.3:c.64A>G	NP_077010.1:p.Thr22Ala
XM_011530369.1:c.64A>G	XP_011528671.1:p.Thr22Ala
XM_011530370.1:c.64A>G	XP_011528672.1:p.Thr22Ala
XM_011530371.1:c.64A>G	XP_011528673.1:p.Thr22Ala
XM_011530371.2:c.64A>G	XP_011528673.1:p.Thr22Ala
XM_017028936.1:c.64A>G	XP_016884425.1:p.Thr22Ala
XM_017028937.1:c.64A>G	XP_016884426.1:p.Thr22Ala
NM_024105.4:c.64A>G MANE Select	NP_077010.1:p.Thr22Ala