Canonical Allele Identifier: CA390746223

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88412023T>C (hg19) ; chr14:g.87945679T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945679T>C , CM000676.2:g.87945679T>C	GRCh38
NC_000014.8:g.88412023T>C , CM000676.1:g.88412023T>C	GRCh37
NC_000014.7:g.87481776T>C	NCBI36
NG_011853.2:g.52885A>G
NG_011853.3:g.52885A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1544A>G MANE Select	ENSP00000261304.2:p.Glu515Gly
ENST00000261304.6:c.1544A>G	ENSP00000261304.2:p.Glu515Gly
ENST00000393568.8:c.1475A>G	ENSP00000377198.4:p.Glu492Gly
ENST00000393569.6:c.1466A>G	ENSP00000377199.2:p.Glu489Gly
ENST00000544807.6:c.1376A>G	ENSP00000437513.2:p.Glu459Gly
ENST00000555000.5:c.911A>G	ENSP00000450472.1:p.Glu304Gly
ENST00000555179.1:c.206+2049A>G
ENST00000557316.5:c.*942A>G	ENSP00000452314.1:n.*942A>G
NM_000153.3:c.1544A>G	NP_000144.2:p.Glu515Gly
NM_001201401.1:c.1475A>G	NP_001188330.1:p.Glu492Gly
NM_001201402.1:c.1466A>G	NP_001188331.1:p.Glu489Gly
XM_011536618.1:c.1376A>G	XP_011534920.1:p.Glu459Gly
XM_011536618.2:c.1376A>G	XP_011534920.1:p.Glu459Gly
NM_000153.4:c.1544A>G MANE Select	NP_000144.2:p.Glu515Gly
NM_001201401.2:c.1475A>G	NP_001188330.1:p.Glu492Gly
NM_001201402.2:c.1466A>G	NP_001188331.1:p.Glu489Gly