Canonical Allele Identifier: CA2153349657
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87933163T= , CM000676.2:g.87933163T= GRCh38
NC_000014.8:g.88399507T= , CM000676.1:g.88399507T= GRCh37
NC_000014.7:g.87469260T= NCBI36
NG_011853.2:g.65401A=
NG_011853.3:g.65401A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.*1569A= MANE Select ENSP00000261304.2:n.*1569A=
ENST00000261304.6:c.*1569A= ENSP00000261304.2:n.*1569A=
ENST00000555000.5:c.*74+736A= ENSP00000450472.1:n.*74+736A=
NM_000153.3:c.*1569A= NP_000144.2:n.*1569A=
NM_001201401.1:c.*1569A= NP_001188330.1:n.*1569A=
NM_001201402.1:c.*1569A= NP_001188331.1:n.*1569A=
XM_011536618.1:c.*1569A= XP_011534920.1:n.*1569A=
XM_011536618.2:c.*1569A= XP_011534920.1:n.*1569A=
NM_000153.4:c.*1569A= MANE Select NP_000144.2:n.*1569A=
NM_001201401.2:c.*1569A= NP_001188330.1:n.*1569A=
NM_001201402.2:c.*1569A= NP_001188331.1:n.*1569A=