Canonical Allele Identifier: CA390745893
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87941540C>G , CM000676.2:g.87941540C>G GRCh38
NC_000014.8:g.88407884C>G , CM000676.1:g.88407884C>G GRCh37
NC_000014.7:g.87477637C>G NCBI36
NG_011853.2:g.57024G>C
NG_011853.3:g.57024G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.1689G>C MANE Select ENSP00000261304.2:p.Lys563Asn
ENST00000261304.6:c.1689G>C ENSP00000261304.2:p.Lys563Asn
ENST00000393568.8:c.1620G>C ENSP00000377198.4:p.Lys540Asn
ENST00000393569.6:c.1611G>C ENSP00000377199.2:p.Lys537Asn
ENST00000544807.6:c.1521G>C ENSP00000437513.2:p.Lys507Asn
ENST00000555000.5:c.1056G>C ENSP00000450472.1:p.Lys352Asn
ENST00000555179.1:c.225G>C
ENST00000557316.5:c.*1087G>C ENSP00000452314.1:n.*1087G>C
NM_000153.3:c.1689G>C NP_000144.2:p.Lys563Asn
NM_001201401.1:c.1620G>C NP_001188330.1:p.Lys540Asn
NM_001201402.1:c.1611G>C NP_001188331.1:p.Lys537Asn
XM_011536618.1:c.1521G>C XP_011534920.1:p.Lys507Asn
XM_011536618.2:c.1521G>C XP_011534920.1:p.Lys507Asn
NM_000153.4:c.1689G>C MANE Select NP_000144.2:p.Lys563Asn
NM_001201401.2:c.1620G>C NP_001188330.1:p.Lys540Asn
NM_001201402.2:c.1611G>C NP_001188331.1:p.Lys537Asn