Canonical Allele Identifier: CA2625980218
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87968231_87968232del , CM000676.2:g.87968231_87968232del GRCh38
NC_000014.8:g.88434575_88434576del , CM000676.1:g.88434575_88434576del GRCh37
NC_000014.7:g.87504328_87504329del NCBI36
NG_011853.2:g.30332_30333del
NG_011853.3:g.30332_30333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.908+103_908+104del MANE Select ENSP00000261304.2:n.908+103_908+104del
ENST00000261304.6:c.908+103_908+104del ENSP00000261304.2:n.908+103_908+104del
ENST00000393568.8:c.839+103_839+104del ENSP00000377198.4:n.839+103_839+104del
ENST00000393569.6:c.830+103_830+104del ENSP00000377199.2:n.830+103_830+104del
ENST00000474294.6:n.898+103_898+104del
ENST00000544807.6:c.740+103_740+104del ENSP00000437513.2:n.740+103_740+104del
ENST00000555000.5:c.275+103_275+104del ENSP00000450472.1:n.275+103_275+104del
ENST00000557316.5:c.*306+103_*306+104del ENSP00000452314.1:n.*306+103_*306+104del
ENST00000622264.4:c.898+103_898+104del
NM_000153.3:c.908+103_908+104del NP_000144.2:n.908+103_908+104del
NM_001201401.1:c.839+103_839+104del NP_001188330.1:n.839+103_839+104del
NM_001201402.1:c.830+103_830+104del NP_001188331.1:n.830+103_830+104del
XM_011536618.1:c.740+103_740+104del XP_011534920.1:n.740+103_740+104del
XM_011536618.2:c.740+103_740+104del XP_011534920.1:n.740+103_740+104del
NM_000153.4:c.908+103_908+104del MANE Select NP_000144.2:n.908+103_908+104del
NM_001201401.2:c.839+103_839+104del NP_001188330.1:n.839+103_839+104del
NM_001201402.2:c.830+103_830+104del NP_001188331.1:n.830+103_830+104del