Canonical Allele Identifier: CA2153345231
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87965597T= , CM000676.2:g.87965597T= GRCh38
NC_000014.8:g.88431941T= , CM000676.1:g.88431941T= GRCh37
NC_000014.7:g.87501694T= NCBI36
NG_011853.2:g.32967A=
NG_011853.3:g.32967A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.941A= MANE Select ENSP00000261304.2:p.Tyr314=
ENST00000261304.6:c.941A= ENSP00000261304.2:p.Tyr314=
ENST00000393568.8:c.872A= ENSP00000377198.4:p.Tyr291=
ENST00000393569.6:c.863A= ENSP00000377199.2:p.Tyr288=
ENST00000474294.6:n.931A=
ENST00000544807.6:c.773A= ENSP00000437513.2:p.Tyr258=
ENST00000555000.5:c.308A= ENSP00000450472.1:p.Tyr103=
ENST00000557316.5:c.*339A= ENSP00000452314.1:n.*339A=
ENST00000557520.1:n.27A=
ENST00000622264.4:c.931A=
NM_000153.3:c.941A= NP_000144.2:p.Tyr314=
NM_001201401.1:c.872A= NP_001188330.1:p.Tyr291=
NM_001201402.1:c.863A= NP_001188331.1:p.Tyr288=
XM_011536618.1:c.773A= XP_011534920.1:p.Tyr258=
XM_011536618.2:c.773A= XP_011534920.1:p.Tyr258=
NM_000153.4:c.941A= MANE Select NP_000144.2:p.Tyr314=
NM_001201401.2:c.872A= NP_001188330.1:p.Tyr291=
NM_001201402.2:c.863A= NP_001188331.1:p.Tyr288=