Canonical Allele Identifier: CA2153381807
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976482T= , CM000676.2:g.87976482T= GRCh38
NC_000014.8:g.88442826T= , CM000676.1:g.88442826T= GRCh37
NC_000014.7:g.87512579T= NCBI36
NG_011853.2:g.22082A=
NG_011853.3:g.22082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.628A= MANE Select ENSP00000261304.2:p.Arg210=
ENST00000261304.6:c.628A= ENSP00000261304.2:p.Arg210=
ENST00000393568.8:c.559A= ENSP00000377198.4:p.Arg187=
ENST00000393569.6:c.550A= ENSP00000377199.2:p.Arg184=
ENST00000474294.6:n.618A=
ENST00000477716.3:n.383A=
ENST00000544807.6:c.460A= ENSP00000437513.2:p.Arg154=
ENST00000554916.5:n.507A=
ENST00000555000.5:c.-6A= ENSP00000450472.1:n.-6A=
ENST00000557316.5:c.*26A= ENSP00000452314.1:n.*26A=
ENST00000622264.4:c.618A=
NM_000153.3:c.628A= NP_000144.2:p.Arg210=
NM_001201401.1:c.559A= NP_001188330.1:p.Arg187=
NM_001201402.1:c.550A= NP_001188331.1:p.Arg184=
XM_011536618.1:c.460A= XP_011534920.1:p.Arg154=
XM_011536618.2:c.460A= XP_011534920.1:p.Arg154=
NM_000153.4:c.628A= MANE Select NP_000144.2:p.Arg210=
NM_001201401.2:c.559A= NP_001188330.1:p.Arg187=
NM_001201402.2:c.550A= NP_001188331.1:p.Arg184=