Canonical Allele Identifier: CA487366312

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442826T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976482T>G , CM000676.2:g.87976482T>G	GRCh38
NC_000014.8:g.88442826T>G , CM000676.1:g.88442826T>G	GRCh37
NC_000014.7:g.87512579T>G	NCBI36
NG_011853.2:g.22082A>C
NG_011853.3:g.22082A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.628A>C MANE Select	ENSP00000261304.2:p.Arg210=
ENST00000261304.6:c.628A>C	ENSP00000261304.2:p.Arg210=
ENST00000393568.8:c.559A>C	ENSP00000377198.4:p.Arg187=
ENST00000393569.6:c.550A>C	ENSP00000377199.2:p.Arg184=
ENST00000474294.6:n.618A>C
ENST00000477716.3:n.383A>C
ENST00000544807.6:c.460A>C	ENSP00000437513.2:p.Arg154=
ENST00000554916.5:n.507A>C
ENST00000555000.5:c.-6A>C	ENSP00000450472.1:n.-6A>C
ENST00000557316.5:c.*26A>C	ENSP00000452314.1:n.*26A>C
ENST00000622264.4:c.618A>C
NM_000153.3:c.628A>C	NP_000144.2:p.Arg210=
NM_001201401.1:c.559A>C	NP_001188330.1:p.Arg187=
NM_001201402.1:c.550A>C	NP_001188331.1:p.Arg184=
XM_011536618.1:c.460A>C	XP_011534920.1:p.Arg154=
XM_011536618.2:c.460A>C	XP_011534920.1:p.Arg154=
NM_000153.4:c.628A>C MANE Select	NP_000144.2:p.Arg210=
NM_001201401.2:c.559A>C	NP_001188330.1:p.Arg187=
NM_001201402.2:c.550A>C	NP_001188331.1:p.Arg184=