Canonical Allele Identifier: CA2153381809
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976485A= , CM000676.2:g.87976485A= GRCh38
NC_000014.8:g.88442829A= , CM000676.1:g.88442829A= GRCh37
NC_000014.7:g.87512582A= NCBI36
NG_011853.2:g.22079T=
NG_011853.3:g.22079T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.625T= MANE Select ENSP00000261304.2:p.Leu209=
ENST00000261304.6:c.625T= ENSP00000261304.2:p.Leu209=
ENST00000393568.8:c.556T= ENSP00000377198.4:p.Leu186=
ENST00000393569.6:c.547T= ENSP00000377199.2:p.Leu183=
ENST00000474294.6:n.615T=
ENST00000477716.3:n.380T=
ENST00000544807.6:c.457T= ENSP00000437513.2:p.Leu153=
ENST00000554916.5:n.504T=
ENST00000555000.5:c.-9T= ENSP00000450472.1:n.-9T=
ENST00000557316.5:c.*23T= ENSP00000452314.1:n.*23T=
ENST00000622264.4:c.615T=
NM_000153.3:c.625T= NP_000144.2:p.Leu209=
NM_001201401.1:c.556T= NP_001188330.1:p.Leu186=
NM_001201402.1:c.547T= NP_001188331.1:p.Leu183=
XM_011536618.1:c.457T= XP_011534920.1:p.Leu153=
XM_011536618.2:c.457T= XP_011534920.1:p.Leu153=
NM_000153.4:c.625T= MANE Select NP_000144.2:p.Leu209=
NM_001201401.2:c.556T= NP_001188330.1:p.Leu186=
NM_001201402.2:c.547T= NP_001188331.1:p.Leu183=