Canonical Allele Identifier: CA390746275

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88412047A>C (hg19) ; chr14:g.87945703A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945703A>C , CM000676.2:g.87945703A>C	GRCh38
NC_000014.8:g.88412047A>C , CM000676.1:g.88412047A>C	GRCh37
NC_000014.7:g.87481800A>C	NCBI36
NG_011853.2:g.52861T>G
NG_011853.3:g.52861T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1520T>G MANE Select	ENSP00000261304.2:p.Phe507Cys
ENST00000261304.6:c.1520T>G	ENSP00000261304.2:p.Phe507Cys
ENST00000393568.8:c.1451T>G	ENSP00000377198.4:p.Phe484Cys
ENST00000393569.6:c.1442T>G	ENSP00000377199.2:p.Phe481Cys
ENST00000544807.6:c.1352T>G	ENSP00000437513.2:p.Phe451Cys
ENST00000555000.5:c.887T>G	ENSP00000450472.1:p.Phe296Cys
ENST00000555179.1:c.206+2025T>G
ENST00000557316.5:c.*918T>G	ENSP00000452314.1:n.*918T>G
NM_000153.3:c.1520T>G	NP_000144.2:p.Phe507Cys
NM_001201401.1:c.1451T>G	NP_001188330.1:p.Phe484Cys
NM_001201402.1:c.1442T>G	NP_001188331.1:p.Phe481Cys
XM_011536618.1:c.1352T>G	XP_011534920.1:p.Phe451Cys
XM_011536618.2:c.1352T>G	XP_011534920.1:p.Phe451Cys
NM_000153.4:c.1520T>G MANE Select	NP_000144.2:p.Phe507Cys
NM_001201401.2:c.1451T>G	NP_001188330.1:p.Phe484Cys
NM_001201402.2:c.1442T>G	NP_001188331.1:p.Phe481Cys