Canonical Allele Identifier: CA390746296

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88412056G>A (hg19) ; chr14:g.87945712G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945712G>A , CM000676.2:g.87945712G>A	GRCh38
NC_000014.8:g.88412056G>A , CM000676.1:g.88412056G>A	GRCh37
NC_000014.7:g.87481809G>A	NCBI36
NG_011853.2:g.52852C>T
NG_011853.3:g.52852C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1511C>T MANE Select	ENSP00000261304.2:p.Ala504Val
ENST00000261304.6:c.1511C>T	ENSP00000261304.2:p.Ala504Val
ENST00000393568.8:c.1442C>T	ENSP00000377198.4:p.Ala481Val
ENST00000393569.6:c.1433C>T	ENSP00000377199.2:p.Ala478Val
ENST00000544807.6:c.1343C>T	ENSP00000437513.2:p.Ala448Val
ENST00000555000.5:c.878C>T	ENSP00000450472.1:p.Ala293Val
ENST00000555179.1:c.206+2016C>T
ENST00000557316.5:c.*909C>T	ENSP00000452314.1:n.*909C>T
NM_000153.3:c.1511C>T	NP_000144.2:p.Ala504Val
NM_001201401.1:c.1442C>T	NP_001188330.1:p.Ala481Val
NM_001201402.1:c.1433C>T	NP_001188331.1:p.Ala478Val
XM_011536618.1:c.1343C>T	XP_011534920.1:p.Ala448Val
XM_011536618.2:c.1343C>T	XP_011534920.1:p.Ala448Val
NM_000153.4:c.1511C>T MANE Select	NP_000144.2:p.Ala504Val
NM_001201401.2:c.1442C>T	NP_001188330.1:p.Ala481Val
NM_001201402.2:c.1433C>T	NP_001188331.1:p.Ala478Val