Canonical Allele Identifier: CA2153350313
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87934733T= , CM000676.2:g.87934733T= GRCh38
NC_000014.8:g.88401077T= , CM000676.1:g.88401077T= GRCh37
NC_000014.7:g.87470830T= NCBI36
NG_011853.2:g.63831A=
NG_011853.3:g.63831A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.2057A= MANE Select ENSP00000261304.2:p.Ter686=
ENST00000261304.6:c.2057A= ENSP00000261304.2:p.Ter686=
ENST00000393568.8:c.1988A= ENSP00000377198.4:p.Ter663=
ENST00000393569.6:c.1979A= ENSP00000377199.2:p.Ter660=
ENST00000544807.6:c.1744-734A= ENSP00000437513.2:n.1744-734A=
ENST00000555000.5:c.1279-734A= ENSP00000450472.1:n.1279-734A=
NM_000153.3:c.2057A= NP_000144.2:p.Ter686=
NM_001201401.1:c.1988A= NP_001188330.1:p.Ter663=
NM_001201402.1:c.1979A= NP_001188331.1:p.Ter660=
XM_011536618.1:c.1889A= XP_011534920.1:p.Ter630=
XM_011536618.2:c.1889A= XP_011534920.1:p.Ter630=
NM_000153.4:c.2057A= MANE Select NP_000144.2:p.Ter686=
NM_001201401.2:c.1988A= NP_001188330.1:p.Ter663=
NM_001201402.2:c.1979A= NP_001188331.1:p.Ter660=