Canonical Allele Identifier: CA487355607

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414079G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947735G>A , CM000676.2:g.87947735G>A	GRCh38
NC_000014.8:g.88414079G>A , CM000676.1:g.88414079G>A	GRCh37
NC_000014.7:g.87483832G>A	NCBI36
NG_011853.2:g.50829C>T
NG_011853.3:g.50829C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1482C>T MANE Select	ENSP00000261304.2:p.Phe494=
ENST00000261304.6:c.1482C>T	ENSP00000261304.2:p.Phe494=
ENST00000393568.8:c.1413C>T	ENSP00000377198.4:p.Phe471=
ENST00000393569.6:c.1404C>T	ENSP00000377199.2:p.Phe468=
ENST00000544807.6:c.1314C>T	ENSP00000437513.2:p.Phe438=
ENST00000555000.5:c.849C>T	ENSP00000450472.1:p.Phe283=
ENST00000555179.1:c.199C>T
ENST00000557316.5:c.*880C>T	ENSP00000452314.1:n.*880C>T
NM_000153.3:c.1482C>T	NP_000144.2:p.Phe494=
NM_001201401.1:c.1413C>T	NP_001188330.1:p.Phe471=
NM_001201402.1:c.1404C>T	NP_001188331.1:p.Phe468=
XM_011536618.1:c.1314C>T	XP_011534920.1:p.Phe438=
XM_011536618.2:c.1314C>T	XP_011534920.1:p.Phe438=
NM_000153.4:c.1482C>T MANE Select	NP_000144.2:p.Phe494=
NM_001201401.2:c.1413C>T	NP_001188330.1:p.Phe471=
NM_001201402.2:c.1404C>T	NP_001188331.1:p.Phe468=