Canonical Allele Identifier: CA390749588

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442780G>A (hg19) ; chr14:g.87976436G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976436G>A , CM000676.2:g.87976436G>A	GRCh38
NC_000014.8:g.88442780G>A , CM000676.1:g.88442780G>A	GRCh37
NC_000014.7:g.87512533G>A	NCBI36
NG_011853.2:g.22128C>T
NG_011853.3:g.22128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.674C>T MANE Select	ENSP00000261304.2:p.Ala225Val
ENST00000261304.6:c.674C>T	ENSP00000261304.2:p.Ala225Val
ENST00000393568.8:c.605C>T	ENSP00000377198.4:p.Ala202Val
ENST00000393569.6:c.596C>T	ENSP00000377199.2:p.Ala199Val
ENST00000474294.6:n.664C>T
ENST00000477716.3:n.429C>T
ENST00000544807.6:c.506C>T	ENSP00000437513.2:p.Ala169Val
ENST00000554916.5:n.553C>T
ENST00000555000.5:c.41C>T	ENSP00000450472.1:p.Ala14Val
ENST00000557316.5:c.*72C>T	ENSP00000452314.1:n.*72C>T
ENST00000622264.4:c.664C>T
NM_000153.3:c.674C>T	NP_000144.2:p.Ala225Val
NM_001201401.1:c.605C>T	NP_001188330.1:p.Ala202Val
NM_001201402.1:c.596C>T	NP_001188331.1:p.Ala199Val
XM_011536618.1:c.506C>T	XP_011534920.1:p.Ala169Val
XM_011536618.2:c.506C>T	XP_011534920.1:p.Ala169Val
NM_000153.4:c.674C>T MANE Select	NP_000144.2:p.Ala225Val
NM_001201401.2:c.605C>T	NP_001188330.1:p.Ala202Val
NM_001201402.2:c.596C>T	NP_001188331.1:p.Ala199Val