Canonical Allele Identifier: CA2153381814
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976502A= , CM000676.2:g.87976502A= GRCh38
NC_000014.8:g.88442846A= , CM000676.1:g.88442846A= GRCh37
NC_000014.7:g.87512599A= NCBI36
NG_011853.2:g.22062T=
NG_011853.3:g.22062T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.622-14T= MANE Select ENSP00000261304.2:n.622-14T=
ENST00000261304.6:c.622-14T= ENSP00000261304.2:n.622-14T=
ENST00000393568.8:c.553-14T= ENSP00000377198.4:n.553-14T=
ENST00000393569.6:c.544-14T= ENSP00000377199.2:n.544-14T=
ENST00000474294.6:n.612-14T=
ENST00000477716.3:n.363T=
ENST00000544807.6:c.454-14T= ENSP00000437513.2:n.454-14T=
ENST00000554916.5:n.501-14T=
ENST00000555000.5:c.-12-14T= ENSP00000450472.1:n.-12-14T=
ENST00000557316.5:c.*20-14T= ENSP00000452314.1:n.*20-14T=
ENST00000622264.4:c.612-14T=
NM_000153.3:c.622-14T= NP_000144.2:n.622-14T=
NM_001201401.1:c.553-14T= NP_001188330.1:n.553-14T=
NM_001201402.1:c.544-14T= NP_001188331.1:n.544-14T=
XM_011536618.1:c.454-14T= XP_011534920.1:n.454-14T=
XM_011536618.2:c.454-14T= XP_011534920.1:n.454-14T=
NM_000153.4:c.622-14T= MANE Select NP_000144.2:n.622-14T=
NM_001201401.2:c.553-14T= NP_001188330.1:n.553-14T=
NM_001201402.2:c.544-14T= NP_001188331.1:n.544-14T=