Canonical Allele Identifier: CA2153350285
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87934653T= , CM000676.2:g.87934653T= GRCh38
NC_000014.8:g.88400997T= , CM000676.1:g.88400997T= GRCh37
NC_000014.7:g.87470750T= NCBI36
NG_011853.2:g.63911A=
NG_011853.3:g.63911A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.*79A= MANE Select ENSP00000261304.2:n.*79A=
ENST00000261304.6:c.*79A= ENSP00000261304.2:n.*79A=
ENST00000393569.6:c.*79A= ENSP00000377199.2:n.*79A=
ENST00000544807.6:c.1744-654A= ENSP00000437513.2:n.1744-654A=
ENST00000555000.5:c.1279-654A= ENSP00000450472.1:n.1279-654A=
NM_000153.3:c.*79A= NP_000144.2:n.*79A=
NM_001201401.1:c.*79A= NP_001188330.1:n.*79A=
NM_001201402.1:c.*79A= NP_001188331.1:n.*79A=
XM_011536618.1:c.*79A= XP_011534920.1:n.*79A=
XM_011536618.2:c.*79A= XP_011534920.1:n.*79A=
NM_000153.4:c.*79A= MANE Select NP_000144.2:n.*79A=
NM_001201401.2:c.*79A= NP_001188330.1:n.*79A=
NM_001201402.2:c.*79A= NP_001188331.1:n.*79A=