Canonical Allele Identifier: CA2153345227
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87965591T= , CM000676.2:g.87965591T= GRCh38
NC_000014.8:g.88431935T= , CM000676.1:g.88431935T= GRCh37
NC_000014.7:g.87501688T= NCBI36
NG_011853.2:g.32973A=
NG_011853.3:g.32973A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.947A= MANE Select ENSP00000261304.2:p.Gln316=
ENST00000261304.6:c.947A= ENSP00000261304.2:p.Gln316=
ENST00000393568.8:c.878A= ENSP00000377198.4:p.Gln293=
ENST00000393569.6:c.869A= ENSP00000377199.2:p.Gln290=
ENST00000474294.6:n.937A=
ENST00000544807.6:c.779A= ENSP00000437513.2:p.Gln260=
ENST00000555000.5:c.314A= ENSP00000450472.1:p.Gln105=
ENST00000557316.5:c.*345A= ENSP00000452314.1:n.*345A=
ENST00000557520.1:n.33A=
ENST00000622264.4:c.937A=
NM_000153.3:c.947A= NP_000144.2:p.Gln316=
NM_001201401.1:c.878A= NP_001188330.1:p.Gln293=
NM_001201402.1:c.869A= NP_001188331.1:p.Gln290=
XM_011536618.1:c.779A= XP_011534920.1:p.Gln260=
XM_011536618.2:c.779A= XP_011534920.1:p.Gln260=
NM_000153.4:c.947A= MANE Select NP_000144.2:p.Gln316=
NM_001201401.2:c.878A= NP_001188330.1:p.Gln293=
NM_001201402.2:c.869A= NP_001188331.1:p.Gln290=