Canonical Allele Identifier: CA487355622

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414106G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947762G>T , CM000676.2:g.87947762G>T	GRCh38
NC_000014.8:g.88414106G>T , CM000676.1:g.88414106G>T	GRCh37
NC_000014.7:g.87483859G>T	NCBI36
NG_011853.2:g.50802C>A
NG_011853.3:g.50802C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1455C>A MANE Select	ENSP00000261304.2:p.Pro485=
ENST00000261304.6:c.1455C>A	ENSP00000261304.2:p.Pro485=
ENST00000393568.8:c.1386C>A	ENSP00000377198.4:p.Pro462=
ENST00000393569.6:c.1377C>A	ENSP00000377199.2:p.Pro459=
ENST00000544807.6:c.1287C>A	ENSP00000437513.2:p.Pro429=
ENST00000555000.5:c.822C>A	ENSP00000450472.1:p.Pro274=
ENST00000555179.1:c.172C>A
ENST00000557316.5:c.*853C>A	ENSP00000452314.1:n.*853C>A
NM_000153.3:c.1455C>A	NP_000144.2:p.Pro485=
NM_001201401.1:c.1386C>A	NP_001188330.1:p.Pro462=
NM_001201402.1:c.1377C>A	NP_001188331.1:p.Pro459=
XM_011536618.1:c.1287C>A	XP_011534920.1:p.Pro429=
XM_011536618.2:c.1287C>A	XP_011534920.1:p.Pro429=
NM_000153.4:c.1455C>A MANE Select	NP_000144.2:p.Pro485=
NM_001201401.2:c.1386C>A	NP_001188330.1:p.Pro462=
NM_001201402.2:c.1377C>A	NP_001188331.1:p.Pro459=