Canonical Allele Identifier: CA487366278

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442773A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976429A>G , CM000676.2:g.87976429A>G	GRCh38
NC_000014.8:g.88442773A>G , CM000676.1:g.88442773A>G	GRCh37
NC_000014.7:g.87512526A>G	NCBI36
NG_011853.2:g.22135T>C
NG_011853.3:g.22135T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.681T>C MANE Select	ENSP00000261304.2:p.Asp227=
ENST00000261304.6:c.681T>C	ENSP00000261304.2:p.Asp227=
ENST00000393568.8:c.612T>C	ENSP00000377198.4:p.Asp204=
ENST00000393569.6:c.603T>C	ENSP00000377199.2:p.Asp201=
ENST00000474294.6:n.671T>C
ENST00000477716.3:n.436T>C
ENST00000544807.6:c.513T>C	ENSP00000437513.2:p.Asp171=
ENST00000554916.5:n.560T>C
ENST00000555000.5:c.48T>C	ENSP00000450472.1:p.Asp16=
ENST00000557316.5:c.*79T>C	ENSP00000452314.1:n.*79T>C
ENST00000622264.4:c.671T>C
NM_000153.3:c.681T>C	NP_000144.2:p.Asp227=
NM_001201401.1:c.612T>C	NP_001188330.1:p.Asp204=
NM_001201402.1:c.603T>C	NP_001188331.1:p.Asp201=
XM_011536618.1:c.513T>C	XP_011534920.1:p.Asp171=
XM_011536618.2:c.513T>C	XP_011534920.1:p.Asp171=
NM_000153.4:c.681T>C MANE Select	NP_000144.2:p.Asp227=
NM_001201401.2:c.612T>C	NP_001188330.1:p.Asp204=
NM_001201402.2:c.603T>C	NP_001188331.1:p.Asp201=