Canonical Allele Identifier: CA390746426

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414099T>A (hg19) ; chr14:g.87947755T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947755T>A , CM000676.2:g.87947755T>A	GRCh38
NC_000014.8:g.88414099T>A , CM000676.1:g.88414099T>A	GRCh37
NC_000014.7:g.87483852T>A	NCBI36
NG_011853.2:g.50809A>T
NG_011853.3:g.50809A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1462A>T MANE Select	ENSP00000261304.2:p.Ser488Cys
ENST00000261304.6:c.1462A>T	ENSP00000261304.2:p.Ser488Cys
ENST00000393568.8:c.1393A>T	ENSP00000377198.4:p.Ser465Cys
ENST00000393569.6:c.1384A>T	ENSP00000377199.2:p.Ser462Cys
ENST00000544807.6:c.1294A>T	ENSP00000437513.2:p.Ser432Cys
ENST00000555000.5:c.829A>T	ENSP00000450472.1:p.Ser277Cys
ENST00000555179.1:c.179A>T
ENST00000557316.5:c.*860A>T	ENSP00000452314.1:n.*860A>T
NM_000153.3:c.1462A>T	NP_000144.2:p.Ser488Cys
NM_001201401.1:c.1393A>T	NP_001188330.1:p.Ser465Cys
NM_001201402.1:c.1384A>T	NP_001188331.1:p.Ser462Cys
XM_011536618.1:c.1294A>T	XP_011534920.1:p.Ser432Cys
XM_011536618.2:c.1294A>T	XP_011534920.1:p.Ser432Cys
NM_000153.4:c.1462A>T MANE Select	NP_000144.2:p.Ser488Cys
NM_001201401.2:c.1393A>T	NP_001188330.1:p.Ser465Cys
NM_001201402.2:c.1384A>T	NP_001188331.1:p.Ser462Cys