Canonical Allele Identifier: CA259863

Gene: GALC

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945593C>T , CM000676.2:g.87945593C>T	GRCh38
NC_000014.8:g.88411937C>T , CM000676.1:g.88411937C>T	GRCh37
NC_000014.7:g.87481690C>T	NCBI36
NG_011853.2:g.52971G>A
NG_011853.3:g.52971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1630G>A MANE Select	ENSP00000261304.2:p.Asp544Asn
ENST00000261304.6:c.1630G>A	ENSP00000261304.2:p.Asp544Asn
ENST00000393568.8:c.1561G>A	ENSP00000377198.4:p.Asp521Asn
ENST00000393569.6:c.1552G>A	ENSP00000377199.2:p.Asp518Asn
ENST00000544807.6:c.1462G>A	ENSP00000437513.2:p.Asp488Asn
ENST00000555000.5:c.997G>A	ENSP00000450472.1:p.Asp333Asn
ENST00000555179.1:c.206+2135G>A
ENST00000557316.5:c.*1028G>A	ENSP00000452314.1:n.*1028G>A
NM_000153.3:c.1630G>A	NP_000144.2:p.Asp544Asn
NM_001201401.1:c.1561G>A	NP_001188330.1:p.Asp521Asn
NM_001201402.1:c.1552G>A	NP_001188331.1:p.Asp518Asn
XM_011536618.1:c.1462G>A	XP_011534920.1:p.Asp488Asn
XM_011536618.2:c.1462G>A	XP_011534920.1:p.Asp488Asn
NM_000153.4:c.1630G>A MANE Select	NP_000144.2:p.Asp544Asn
NM_001201401.2:c.1561G>A	NP_001188330.1:p.Asp521Asn
NM_001201402.2:c.1552G>A	NP_001188331.1:p.Asp518Asn