Canonical Allele Identifier: CA2514766509
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87968319_87968321del , CM000676.2:g.87968319_87968321del GRCh38
NC_000014.8:g.88434663_88434665del , CM000676.1:g.88434663_88434665del GRCh37
NC_000014.7:g.87504416_87504418del NCBI36
NG_011853.2:g.30243_30245del
NG_011853.3:g.30243_30245del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.908+14_908+16del MANE Select ENSP00000261304.2:n.908+14_908+16del
ENST00000261304.6:c.908+14_908+16del ENSP00000261304.2:n.908+14_908+16del
ENST00000393568.8:c.839+14_839+16del ENSP00000377198.4:n.839+14_839+16del
ENST00000393569.6:c.830+14_830+16del ENSP00000377199.2:n.830+14_830+16del
ENST00000474294.6:n.898+14_898+16del
ENST00000544807.6:c.740+14_740+16del ENSP00000437513.2:n.740+14_740+16del
ENST00000555000.5:c.275+14_275+16del ENSP00000450472.1:n.275+14_275+16del
ENST00000557316.5:c.*306+14_*306+16del ENSP00000452314.1:n.*306+14_*306+16del
ENST00000622264.4:c.898+14_898+16del
NM_000153.3:c.908+14_908+16del NP_000144.2:n.908+14_908+16del
NM_001201401.1:c.839+14_839+16del NP_001188330.1:n.839+14_839+16del
NM_001201402.1:c.830+14_830+16del NP_001188331.1:n.830+14_830+16del
XM_011536618.1:c.740+14_740+16del XP_011534920.1:n.740+14_740+16del
XM_011536618.2:c.740+14_740+16del XP_011534920.1:n.740+14_740+16del
NM_000153.4:c.908+14_908+16del MANE Select NP_000144.2:n.908+14_908+16del
NM_001201401.2:c.839+14_839+16del NP_001188330.1:n.839+14_839+16del
NM_001201402.2:c.830+14_830+16del NP_001188331.1:n.830+14_830+16del