Canonical Allele Identifier: CA487366262

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442755G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976411G>T , CM000676.2:g.87976411G>T	GRCh38
NC_000014.8:g.88442755G>T , CM000676.1:g.88442755G>T	GRCh37
NC_000014.7:g.87512508G>T	NCBI36
NG_011853.2:g.22153C>A
NG_011853.3:g.22153C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.699C>A MANE Select	ENSP00000261304.2:p.Ile233=
ENST00000261304.6:c.699C>A	ENSP00000261304.2:p.Ile233=
ENST00000393568.8:c.630C>A	ENSP00000377198.4:p.Ile210=
ENST00000393569.6:c.621C>A	ENSP00000377199.2:p.Ile207=
ENST00000474294.6:n.689C>A
ENST00000477716.3:n.454C>A
ENST00000544807.6:c.531C>A	ENSP00000437513.2:p.Ile177=
ENST00000554916.5:n.578C>A
ENST00000555000.5:c.66C>A	ENSP00000450472.1:p.Ile22=
ENST00000557316.5:c.*97C>A	ENSP00000452314.1:n.*97C>A
ENST00000622264.4:c.689C>A
NM_000153.3:c.699C>A	NP_000144.2:p.Ile233=
NM_001201401.1:c.630C>A	NP_001188330.1:p.Ile210=
NM_001201402.1:c.621C>A	NP_001188331.1:p.Ile207=
XM_011536618.1:c.531C>A	XP_011534920.1:p.Ile177=
XM_011536618.2:c.531C>A	XP_011534920.1:p.Ile177=
NM_000153.4:c.699C>A MANE Select	NP_000144.2:p.Ile233=
NM_001201401.2:c.630C>A	NP_001188330.1:p.Ile210=
NM_001201402.2:c.621C>A	NP_001188331.1:p.Ile207=