Canonical Allele Identifier: CA390745676

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88407784A>T (hg19) ; chr14:g.87941440A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87941440A>T , CM000676.2:g.87941440A>T	GRCh38
NC_000014.8:g.88407784A>T , CM000676.1:g.88407784A>T	GRCh37
NC_000014.7:g.87477537A>T	NCBI36
NG_011853.2:g.57124T>A
NG_011853.3:g.57124T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1789T>A MANE Select	ENSP00000261304.2:p.Phe597Ile
ENST00000261304.6:c.1789T>A	ENSP00000261304.2:p.Phe597Ile
ENST00000393568.8:c.1720T>A	ENSP00000377198.4:p.Phe574Ile
ENST00000393569.6:c.1711T>A	ENSP00000377199.2:p.Phe571Ile
ENST00000544807.6:c.1621T>A	ENSP00000437513.2:p.Phe541Ile
ENST00000555000.5:c.1156T>A	ENSP00000450472.1:p.Phe386Ile
ENST00000555179.1:c.325T>A
ENST00000557316.5:c.*1187T>A	ENSP00000452314.1:n.*1187T>A
NM_000153.3:c.1789T>A	NP_000144.2:p.Phe597Ile
NM_001201401.1:c.1720T>A	NP_001188330.1:p.Phe574Ile
NM_001201402.1:c.1711T>A	NP_001188331.1:p.Phe571Ile
XM_011536618.1:c.1621T>A	XP_011534920.1:p.Phe541Ile
XM_011536618.2:c.1621T>A	XP_011534920.1:p.Phe541Ile
NM_000153.4:c.1789T>A MANE Select	NP_000144.2:p.Phe597Ile
NM_001201401.2:c.1720T>A	NP_001188330.1:p.Phe574Ile
NM_001201402.2:c.1711T>A	NP_001188331.1:p.Phe571Ile