Canonical Allele Identifier: CA390749606

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442786A>T (hg19) ; chr14:g.87976442A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976442A>T , CM000676.2:g.87976442A>T	GRCh38
NC_000014.8:g.88442786A>T , CM000676.1:g.88442786A>T	GRCh37
NC_000014.7:g.87512539A>T	NCBI36
NG_011853.2:g.22122T>A
NG_011853.3:g.22122T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.668T>A MANE Select	ENSP00000261304.2:p.Ile223Asn
ENST00000261304.6:c.668T>A	ENSP00000261304.2:p.Ile223Asn
ENST00000393568.8:c.599T>A	ENSP00000377198.4:p.Ile200Asn
ENST00000393569.6:c.590T>A	ENSP00000377199.2:p.Ile197Asn
ENST00000474294.6:n.658T>A
ENST00000477716.3:n.423T>A
ENST00000544807.6:c.500T>A	ENSP00000437513.2:p.Ile167Asn
ENST00000554916.5:n.547T>A
ENST00000555000.5:c.35T>A	ENSP00000450472.1:p.Ile12Asn
ENST00000557316.5:c.*66T>A	ENSP00000452314.1:n.*66T>A
ENST00000622264.4:c.658T>A
NM_000153.3:c.668T>A	NP_000144.2:p.Ile223Asn
NM_001201401.1:c.599T>A	NP_001188330.1:p.Ile200Asn
NM_001201402.1:c.590T>A	NP_001188331.1:p.Ile197Asn
XM_011536618.1:c.500T>A	XP_011534920.1:p.Ile167Asn
XM_011536618.2:c.500T>A	XP_011534920.1:p.Ile167Asn
NM_000153.4:c.668T>A MANE Select	NP_000144.2:p.Ile223Asn
NM_001201401.2:c.599T>A	NP_001188330.1:p.Ile200Asn
NM_001201402.2:c.590T>A	NP_001188331.1:p.Ile197Asn