Canonical Allele Identifier: CA2153387466
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87988532A= , CM000676.2:g.87988532A= GRCh38
NC_000014.8:g.88454876A= , CM000676.1:g.88454876A= GRCh37
NC_000014.7:g.87524629A= NCBI36
NG_011853.2:g.10032T=
NG_011853.3:g.10032T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.196-9T= MANE Select ENSP00000261304.2:n.196-9T=
ENST00000261304.6:c.196-9T= ENSP00000261304.2:n.196-9T=
ENST00000393568.8:c.196-325T= ENSP00000377198.4:n.196-325T=
ENST00000393569.6:c.118-9T= ENSP00000377199.2:n.118-9T=
ENST00000474294.6:n.186-9T=
ENST00000544807.6:c.28-9T= ENSP00000437513.2:n.28-9T=
ENST00000554372.5:c.196-9T= ENSP00000451884.1:n.196-9T=
ENST00000554916.5:n.75-9T=
ENST00000556879.5:c.256-9T= ENSP00000452208.1:n.256-9T=
ENST00000557316.5:c.196-9T= ENSP00000452314.1:n.196-9T=
ENST00000622264.4:c.186-9T=
NM_000153.3:c.196-9T= NP_000144.2:n.196-9T=
NM_001201401.1:c.196-325T= NP_001188330.1:n.196-325T=
NM_001201402.1:c.118-9T= NP_001188331.1:n.118-9T=
XM_011536618.1:c.28-9T= XP_011534920.1:n.28-9T=
XM_011536618.2:c.28-9T= XP_011534920.1:n.28-9T=
NM_000153.4:c.196-9T= MANE Select NP_000144.2:n.196-9T=
NM_001201401.2:c.196-325T= NP_001188330.1:n.196-325T=
NM_001201402.2:c.118-9T= NP_001188331.1:n.118-9T=