Canonical Allele Identifier: CA390745892
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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