Canonical Allele Identifier: CA2153387458
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87988514G= , CM000676.2:g.87988514G= GRCh38
NC_000014.8:g.88454858G= , CM000676.1:g.88454858G= GRCh37
NC_000014.7:g.87524611G= NCBI36
NG_011853.2:g.10050C=
NG_011853.3:g.10050C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.205C= MANE Select ENSP00000261304.2:p.Arg69=
ENST00000261304.6:c.205C= ENSP00000261304.2:p.Arg69=
ENST00000393568.8:c.196-307C= ENSP00000377198.4:n.196-307C=
ENST00000393569.6:c.127C= ENSP00000377199.2:p.Arg43=
ENST00000474294.6:n.195C=
ENST00000544807.6:c.37C= ENSP00000437513.2:p.Arg13=
ENST00000554372.5:c.205C= ENSP00000451884.1:p.Arg69=
ENST00000554916.5:n.84C=
ENST00000555956.1:n.10C=
ENST00000556879.5:c.265C= ENSP00000452208.1:n.265C=
ENST00000557316.5:c.205C= ENSP00000452314.1:p.Arg69=
ENST00000622264.4:c.195C=
NM_000153.3:c.205C= NP_000144.2:p.Arg69=
NM_001201401.1:c.196-307C= NP_001188330.1:n.196-307C=
NM_001201402.1:c.127C= NP_001188331.1:p.Arg43=
XM_011536618.1:c.37C= XP_011534920.1:p.Arg13=
XM_011536618.2:c.37C= XP_011534920.1:p.Arg13=
NM_000153.4:c.205C= MANE Select NP_000144.2:p.Arg69=
NM_001201401.2:c.196-307C= NP_001188330.1:n.196-307C=
NM_001201402.2:c.127C= NP_001188331.1:p.Arg43=