Canonical Allele Identifier: CA390752470
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87986527T>G , CM000676.2:g.87986527T>G GRCh38
NC_000014.8:g.88452871T>G , CM000676.1:g.88452871T>G GRCh37
NC_000014.7:g.87522624T>G NCBI36
NG_011853.2:g.12037A>C
NG_011853.3:g.12037A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.404A>C MANE Select ENSP00000261304.2:p.Lys135Thr
ENST00000261304.6:c.404A>C ENSP00000261304.2:p.Lys135Thr
ENST00000393568.8:c.335A>C ENSP00000377198.4:p.Lys112Thr
ENST00000393569.6:c.326A>C ENSP00000377199.2:p.Lys109Thr
ENST00000474294.6:n.394A>C
ENST00000544807.6:c.236A>C ENSP00000437513.2:p.Lys79Thr
ENST00000554372.5:c.*153A>C ENSP00000451884.1:n.*153A>C
ENST00000554916.5:n.283A>C
ENST00000556261.5:n.105A>C
ENST00000556879.5:c.464A>C ENSP00000452208.1:n.464A>C
ENST00000557316.5:c.404A>C ENSP00000452314.1:p.Lys135Thr
ENST00000622264.4:c.394A>C
NM_000153.3:c.404A>C NP_000144.2:p.Lys135Thr
NM_001201401.1:c.335A>C NP_001188330.1:p.Lys112Thr
NM_001201402.1:c.326A>C NP_001188331.1:p.Lys109Thr
XM_011536618.1:c.236A>C XP_011534920.1:p.Lys79Thr
XM_011536618.2:c.236A>C XP_011534920.1:p.Lys79Thr
NM_000153.4:c.404A>C MANE Select NP_000144.2:p.Lys135Thr
NM_001201401.2:c.335A>C NP_001188330.1:p.Lys112Thr
NM_001201402.2:c.326A>C NP_001188331.1:p.Lys109Thr