Canonical Allele Identifier: CA390745885

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88407881A>T (hg19) ; chr14:g.87941537A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87941537A>T , CM000676.2:g.87941537A>T	GRCh38
NC_000014.8:g.88407881A>T , CM000676.1:g.88407881A>T	GRCh37
NC_000014.7:g.87477634A>T	NCBI36
NG_011853.2:g.57027T>A
NG_011853.3:g.57027T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1692T>A MANE Select	ENSP00000261304.2:p.Cys564Ter
ENST00000261304.6:c.1692T>A	ENSP00000261304.2:p.Cys564Ter
ENST00000393568.8:c.1623T>A	ENSP00000377198.4:p.Cys541Ter
ENST00000393569.6:c.1614T>A	ENSP00000377199.2:p.Cys538Ter
ENST00000544807.6:c.1524T>A	ENSP00000437513.2:p.Cys508Ter
ENST00000555000.5:c.1059T>A	ENSP00000450472.1:p.Cys353Ter
ENST00000555179.1:c.228T>A
ENST00000557316.5:c.*1090T>A	ENSP00000452314.1:n.*1090T>A
NM_000153.3:c.1692T>A	NP_000144.2:p.Cys564Ter
NM_001201401.1:c.1623T>A	NP_001188330.1:p.Cys541Ter
NM_001201402.1:c.1614T>A	NP_001188331.1:p.Cys538Ter
XM_011536618.1:c.1524T>A	XP_011534920.1:p.Cys508Ter
XM_011536618.2:c.1524T>A	XP_011534920.1:p.Cys508Ter
NM_000153.4:c.1692T>A MANE Select	NP_000144.2:p.Cys564Ter
NM_001201401.2:c.1623T>A	NP_001188330.1:p.Cys541Ter
NM_001201402.2:c.1614T>A	NP_001188331.1:p.Cys538Ter