Canonical Allele Identifier: CA2153381758
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976386C= , CM000676.2:g.87976386C= GRCh38
NC_000014.8:g.88442730C= , CM000676.1:g.88442730C= GRCh37
NC_000014.7:g.87512483C= NCBI36
NG_011853.2:g.22178G=
NG_011853.3:g.22178G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.724G= MANE Select ENSP00000261304.2:p.Glu242=
ENST00000261304.6:c.724G= ENSP00000261304.2:p.Glu242=
ENST00000393568.8:c.655G= ENSP00000377198.4:p.Glu219=
ENST00000393569.6:c.646G= ENSP00000377199.2:p.Glu216=
ENST00000474294.6:n.714G=
ENST00000477716.3:n.479G=
ENST00000544807.6:c.556G= ENSP00000437513.2:p.Glu186=
ENST00000554916.5:n.603G=
ENST00000555000.5:c.91G= ENSP00000450472.1:p.Glu31=
ENST00000557316.5:c.*122G= ENSP00000452314.1:n.*122G=
ENST00000622264.4:c.714G=
NM_000153.3:c.724G= NP_000144.2:p.Glu242=
NM_001201401.1:c.655G= NP_001188330.1:p.Glu219=
NM_001201402.1:c.646G= NP_001188331.1:p.Glu216=
XM_011536618.1:c.556G= XP_011534920.1:p.Glu186=
XM_011536618.2:c.556G= XP_011534920.1:p.Glu186=
NM_000153.4:c.724G= MANE Select NP_000144.2:p.Glu242=
NM_001201401.2:c.655G= NP_001188330.1:p.Glu219=
NM_001201402.2:c.646G= NP_001188331.1:p.Glu216=