Canonical Allele Identifier: CA390749577

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442776A>C (hg19) ; chr14:g.87976432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976432A>C , CM000676.2:g.87976432A>C	GRCh38
NC_000014.8:g.88442776A>C , CM000676.1:g.88442776A>C	GRCh37
NC_000014.7:g.87512529A>C	NCBI36
NG_011853.2:g.22132T>G
NG_011853.3:g.22132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.678T>G MANE Select	ENSP00000261304.2:p.Ser226Arg
ENST00000261304.6:c.678T>G	ENSP00000261304.2:p.Ser226Arg
ENST00000393568.8:c.609T>G	ENSP00000377198.4:p.Ser203Arg
ENST00000393569.6:c.600T>G	ENSP00000377199.2:p.Ser200Arg
ENST00000474294.6:n.668T>G
ENST00000477716.3:n.433T>G
ENST00000544807.6:c.510T>G	ENSP00000437513.2:p.Ser170Arg
ENST00000554916.5:n.557T>G
ENST00000555000.5:c.45T>G	ENSP00000450472.1:p.Ser15Arg
ENST00000557316.5:c.*76T>G	ENSP00000452314.1:n.*76T>G
ENST00000622264.4:c.668T>G
NM_000153.3:c.678T>G	NP_000144.2:p.Ser226Arg
NM_001201401.1:c.609T>G	NP_001188330.1:p.Ser203Arg
NM_001201402.1:c.600T>G	NP_001188331.1:p.Ser200Arg
XM_011536618.1:c.510T>G	XP_011534920.1:p.Ser170Arg
XM_011536618.2:c.510T>G	XP_011534920.1:p.Ser170Arg
NM_000153.4:c.678T>G MANE Select	NP_000144.2:p.Ser226Arg
NM_001201401.2:c.609T>G	NP_001188330.1:p.Ser203Arg
NM_001201402.2:c.600T>G	NP_001188331.1:p.Ser200Arg