Canonical Allele Identifier: CA390745558

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87939979C>T , CM000676.2:g.87939979C>T	GRCh38
NC_000014.8:g.88406323C>T , CM000676.1:g.88406323C>T	GRCh37
NC_000014.7:g.87476076C>T	NCBI36
NG_011853.2:g.58585G>A
NG_011853.3:g.58585G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1837G>A MANE Select	ENSP00000261304.2:p.Gly613Arg
ENST00000261304.6:c.1837G>A	ENSP00000261304.2:p.Gly613Arg
ENST00000393568.8:c.1768G>A	ENSP00000377198.4:p.Gly590Arg
ENST00000393569.6:c.1759G>A	ENSP00000377199.2:p.Gly587Arg
ENST00000544807.6:c.1669G>A	ENSP00000437513.2:p.Gly557Arg
ENST00000555000.5:c.1204G>A	ENSP00000450472.1:p.Gly402Arg
ENST00000555179.1:c.373G>A
NM_000153.3:c.1837G>A	NP_000144.2:p.Gly613Arg
NM_001201401.1:c.1768G>A	NP_001188330.1:p.Gly590Arg
NM_001201402.1:c.1759G>A	NP_001188331.1:p.Gly587Arg
XM_011536618.1:c.1669G>A	XP_011534920.1:p.Gly557Arg
XM_011536618.2:c.1669G>A	XP_011534920.1:p.Gly557Arg
NM_000153.4:c.1837G>A MANE Select	NP_000144.2:p.Gly613Arg
NM_001201401.2:c.1768G>A	NP_001188330.1:p.Gly590Arg
NM_001201402.2:c.1759G>A	NP_001188331.1:p.Gly587Arg