Canonical Allele Identifier: CA390745991

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88411917A>T (hg19) ; chr14:g.87945573A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945573A>T , CM000676.2:g.87945573A>T	GRCh38
NC_000014.8:g.88411917A>T , CM000676.1:g.88411917A>T	GRCh37
NC_000014.7:g.87481670A>T	NCBI36
NG_011853.2:g.52991T>A
NG_011853.3:g.52991T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1650T>A MANE Select	ENSP00000261304.2:p.Ser550Arg
ENST00000261304.6:c.1650T>A	ENSP00000261304.2:p.Ser550Arg
ENST00000393568.8:c.1581T>A	ENSP00000377198.4:p.Ser527Arg
ENST00000393569.6:c.1572T>A	ENSP00000377199.2:p.Ser524Arg
ENST00000544807.6:c.1482T>A	ENSP00000437513.2:p.Ser494Arg
ENST00000555000.5:c.1017T>A	ENSP00000450472.1:p.Ser339Arg
ENST00000555179.1:c.206+2155T>A
ENST00000557316.5:c.*1048T>A	ENSP00000452314.1:n.*1048T>A
NM_000153.3:c.1650T>A	NP_000144.2:p.Ser550Arg
NM_001201401.1:c.1581T>A	NP_001188330.1:p.Ser527Arg
NM_001201402.1:c.1572T>A	NP_001188331.1:p.Ser524Arg
XM_011536618.1:c.1482T>A	XP_011534920.1:p.Ser494Arg
XM_011536618.2:c.1482T>A	XP_011534920.1:p.Ser494Arg
NM_000153.4:c.1650T>A MANE Select	NP_000144.2:p.Ser550Arg
NM_001201401.2:c.1581T>A	NP_001188330.1:p.Ser527Arg
NM_001201402.2:c.1572T>A	NP_001188331.1:p.Ser524Arg