Canonical Allele Identifier: CA2153381761
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87976394A= , CM000676.2:g.87976394A= GRCh38
NC_000014.8:g.88442738A= , CM000676.1:g.88442738A= GRCh37
NC_000014.7:g.87512491A= NCBI36
NG_011853.2:g.22170T=
NG_011853.3:g.22170T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.716T= MANE Select ENSP00000261304.2:p.Leu239=
ENST00000261304.6:c.716T= ENSP00000261304.2:p.Leu239=
ENST00000393568.8:c.647T= ENSP00000377198.4:p.Leu216=
ENST00000393569.6:c.638T= ENSP00000377199.2:p.Leu213=
ENST00000474294.6:n.706T=
ENST00000477716.3:n.471T=
ENST00000544807.6:c.548T= ENSP00000437513.2:p.Leu183=
ENST00000554916.5:n.595T=
ENST00000555000.5:c.83T= ENSP00000450472.1:p.Leu28=
ENST00000557316.5:c.*114T= ENSP00000452314.1:n.*114T=
ENST00000622264.4:c.706T=
NM_000153.3:c.716T= NP_000144.2:p.Leu239=
NM_001201401.1:c.647T= NP_001188330.1:p.Leu216=
NM_001201402.1:c.638T= NP_001188331.1:p.Leu213=
XM_011536618.1:c.548T= XP_011534920.1:p.Leu183=
XM_011536618.2:c.548T= XP_011534920.1:p.Leu183=
NM_000153.4:c.716T= MANE Select NP_000144.2:p.Leu239=
NM_001201401.2:c.647T= NP_001188330.1:p.Leu216=
NM_001201402.2:c.638T= NP_001188331.1:p.Leu213=