Canonical Allele Identifier: CA7296970
Gene: GALC HGNC NCBI

Linked Data

dbSNP Id: rs776857280

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87945599C>G , CM000676.2:g.87945599C>G GRCh38
NC_000014.8:g.88411943C>G , CM000676.1:g.88411943C>G GRCh37
NC_000014.7:g.87481696C>G NCBI36
NG_011853.2:g.52965G>C
NG_011853.3:g.52965G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.1624G>C MANE Select ENSP00000261304.2:p.Ala542Pro
ENST00000261304.6:c.1624G>C ENSP00000261304.2:p.Ala542Pro
ENST00000393568.8:c.1555G>C ENSP00000377198.4:p.Ala519Pro
ENST00000393569.6:c.1546G>C ENSP00000377199.2:p.Ala516Pro
ENST00000544807.6:c.1456G>C ENSP00000437513.2:p.Ala486Pro
ENST00000555000.5:c.991G>C ENSP00000450472.1:p.Ala331Pro
ENST00000555179.1:c.206+2129G>C
ENST00000557316.5:c.*1022G>C ENSP00000452314.1:n.*1022G>C
NM_000153.3:c.1624G>C NP_000144.2:p.Ala542Pro
NM_001201401.1:c.1555G>C NP_001188330.1:p.Ala519Pro
NM_001201402.1:c.1546G>C NP_001188331.1:p.Ala516Pro
XM_011536618.1:c.1456G>C XP_011534920.1:p.Ala486Pro
XM_011536618.2:c.1456G>C XP_011534920.1:p.Ala486Pro
NM_000153.4:c.1624G>C MANE Select NP_000144.2:p.Ala542Pro
NM_001201401.2:c.1555G>C NP_001188330.1:p.Ala519Pro
NM_001201402.2:c.1546G>C NP_001188331.1:p.Ala516Pro