Canonical Allele Identifier: CA390746133

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88411984A>G (hg19) ; chr14:g.87945640A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945640A>G , CM000676.2:g.87945640A>G	GRCh38
NC_000014.8:g.88411984A>G , CM000676.1:g.88411984A>G	GRCh37
NC_000014.7:g.87481737A>G	NCBI36
NG_011853.2:g.52924T>C
NG_011853.3:g.52924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1583T>C MANE Select	ENSP00000261304.2:p.Phe528Ser
ENST00000261304.6:c.1583T>C	ENSP00000261304.2:p.Phe528Ser
ENST00000393568.8:c.1514T>C	ENSP00000377198.4:p.Phe505Ser
ENST00000393569.6:c.1505T>C	ENSP00000377199.2:p.Phe502Ser
ENST00000544807.6:c.1415T>C	ENSP00000437513.2:p.Phe472Ser
ENST00000555000.5:c.950T>C	ENSP00000450472.1:p.Phe317Ser
ENST00000555179.1:c.206+2088T>C
ENST00000557316.5:c.*981T>C	ENSP00000452314.1:n.*981T>C
NM_000153.3:c.1583T>C	NP_000144.2:p.Phe528Ser
NM_001201401.1:c.1514T>C	NP_001188330.1:p.Phe505Ser
NM_001201402.1:c.1505T>C	NP_001188331.1:p.Phe502Ser
XM_011536618.1:c.1415T>C	XP_011534920.1:p.Phe472Ser
XM_011536618.2:c.1415T>C	XP_011534920.1:p.Phe472Ser
NM_000153.4:c.1583T>C MANE Select	NP_000144.2:p.Phe528Ser
NM_001201401.2:c.1514T>C	NP_001188330.1:p.Phe505Ser
NM_001201402.2:c.1505T>C	NP_001188331.1:p.Phe502Ser