Canonical Allele Identifier: CA412080791
Gene: ALG12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50307274T>G (hg19) chr22:g.49913626T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913626T>G , CM000684.2:g.49913626T>G GRCh38
NC_000022.10:g.50307274T>G , CM000684.1:g.50307274T>G GRCh37
NC_000022.9:g.48693278T>G NCBI36
NG_008927.1:g.9833A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.140A>C MANE Select ENSP00000333813.5:p.Tyr47Ser
ENST00000330817.10:c.140A>C ENSP00000333813.5:p.Tyr47Ser
NM_024105.3:c.140A>C NP_077010.1:p.Tyr47Ser
XM_011530369.1:c.140A>C XP_011528671.1:p.Tyr47Ser
XM_011530370.1:c.140A>C XP_011528672.1:p.Tyr47Ser
XM_011530371.1:c.140A>C XP_011528673.1:p.Tyr47Ser
XM_011530371.2:c.140A>C XP_011528673.1:p.Tyr47Ser
XM_017028936.1:c.140A>C XP_016884425.1:p.Tyr47Ser
XM_017028937.1:c.140A>C XP_016884426.1:p.Tyr47Ser
NM_024105.4:c.140A>C MANE Select NP_077010.1:p.Tyr47Ser
Search 100 bp 5'
Search 100 bp 3'