Canonical Allele Identifier: CA2153387460
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87988518G= , CM000676.2:g.87988518G= GRCh38
NC_000014.8:g.88454862G= , CM000676.1:g.88454862G= GRCh37
NC_000014.7:g.87524615G= NCBI36
NG_011853.2:g.10046C=
NG_011853.3:g.10046C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.201C= MANE Select ENSP00000261304.2:p.Thr67=
ENST00000261304.6:c.201C= ENSP00000261304.2:p.Thr67=
ENST00000393568.8:c.196-311C= ENSP00000377198.4:n.196-311C=
ENST00000393569.6:c.123C= ENSP00000377199.2:p.Thr41=
ENST00000474294.6:n.191C=
ENST00000544807.6:c.33C= ENSP00000437513.2:p.Thr11=
ENST00000554372.5:c.201C= ENSP00000451884.1:p.Thr67=
ENST00000554916.5:n.80C=
ENST00000555956.1:n.6C=
ENST00000556879.5:c.261C= ENSP00000452208.1:n.261C=
ENST00000557316.5:c.201C= ENSP00000452314.1:p.Thr67=
ENST00000622264.4:c.191C=
NM_000153.3:c.201C= NP_000144.2:p.Thr67=
NM_001201401.1:c.196-311C= NP_001188330.1:n.196-311C=
NM_001201402.1:c.123C= NP_001188331.1:p.Thr41=
XM_011536618.1:c.33C= XP_011534920.1:p.Thr11=
XM_011536618.2:c.33C= XP_011534920.1:p.Thr11=
NM_000153.4:c.201C= MANE Select NP_000144.2:p.Thr67=
NM_001201401.2:c.196-311C= NP_001188330.1:n.196-311C=
NM_001201402.2:c.123C= NP_001188331.1:p.Thr41=