Canonical Allele Identifier: CA2597552466
Gene: GALC HGNC NCBI

Linked Data

dbSNP Id: rs1886512550

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976795T>A , CM000676.2:g.87976795T>A GRCh38
NC_000014.8:g.88443139T>A , CM000676.1:g.88443139T>A GRCh37
NC_000014.7:g.87512892T>A NCBI36
NG_011853.2:g.21769A>T
NG_011853.3:g.21769A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.622-307A>T MANE Select ENSP00000261304.2:n.622-307A>T
ENST00000261304.6:c.622-307A>T ENSP00000261304.2:n.622-307A>T
ENST00000393568.8:c.553-307A>T ENSP00000377198.4:n.553-307A>T
ENST00000393569.6:c.544-307A>T ENSP00000377199.2:n.544-307A>T
ENST00000474294.6:n.612-307A>T
ENST00000477716.3:n.70A>T
ENST00000544807.6:c.454-307A>T ENSP00000437513.2:n.454-307A>T
ENST00000554916.5:n.501-307A>T
ENST00000555000.5:c.-12-307A>T ENSP00000450472.1:n.-12-307A>T
ENST00000557316.5:c.*20-307A>T ENSP00000452314.1:n.*20-307A>T
ENST00000622264.4:c.612-307A>T
NM_000153.3:c.622-307A>T NP_000144.2:n.622-307A>T
NM_001201401.1:c.553-307A>T NP_001188330.1:n.553-307A>T
NM_001201402.1:c.544-307A>T NP_001188331.1:n.544-307A>T
XM_011536618.1:c.454-307A>T XP_011534920.1:n.454-307A>T
XM_011536618.2:c.454-307A>T XP_011534920.1:n.454-307A>T
NM_000153.4:c.622-307A>T MANE Select NP_000144.2:n.622-307A>T
NM_001201401.2:c.553-307A>T NP_001188330.1:n.553-307A>T
NM_001201402.2:c.544-307A>T NP_001188331.1:n.544-307A>T