Canonical Allele Identifier: CA390749277

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442710A>C (hg19) ; chr14:g.87976366A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976366A>C , CM000676.2:g.87976366A>C	GRCh38
NC_000014.8:g.88442710A>C , CM000676.1:g.88442710A>C	GRCh37
NC_000014.7:g.87512463A>C	NCBI36
NG_011853.2:g.22198T>G
NG_011853.3:g.22198T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.744T>G MANE Select	ENSP00000261304.2:p.Asp248Glu
ENST00000261304.6:c.744T>G	ENSP00000261304.2:p.Asp248Glu
ENST00000393568.8:c.675T>G	ENSP00000377198.4:p.Asp225Glu
ENST00000393569.6:c.666T>G	ENSP00000377199.2:p.Asp222Glu
ENST00000474294.6:n.734T>G
ENST00000477716.3:n.499T>G
ENST00000544807.6:c.576T>G	ENSP00000437513.2:p.Asp192Glu
ENST00000554916.5:n.623T>G
ENST00000555000.5:c.111T>G	ENSP00000450472.1:p.Asp37Glu
ENST00000557316.5:c.*142T>G	ENSP00000452314.1:n.*142T>G
ENST00000622264.4:c.734T>G
NM_000153.3:c.744T>G	NP_000144.2:p.Asp248Glu
NM_001201401.1:c.675T>G	NP_001188330.1:p.Asp225Glu
NM_001201402.1:c.666T>G	NP_001188331.1:p.Asp222Glu
XM_011536618.1:c.576T>G	XP_011534920.1:p.Asp192Glu
XM_011536618.2:c.576T>G	XP_011534920.1:p.Asp192Glu
NM_000153.4:c.744T>G MANE Select	NP_000144.2:p.Asp248Glu
NM_001201401.2:c.675T>G	NP_001188330.1:p.Asp225Glu
NM_001201402.2:c.666T>G	NP_001188331.1:p.Asp222Glu