Canonical Allele Identifier: CA390746735

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87949862G>A , CM000676.2:g.87949862G>A	GRCh38
NC_000014.8:g.88416206G>A , CM000676.1:g.88416206G>A	GRCh37
NC_000014.7:g.87485959G>A	NCBI36
NG_011853.2:g.48702C>T
NG_011853.3:g.48702C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000153.4:c.1321C>T MANE Select	NP_000144.2:p.Gln441Ter
ENST00000261304.7:c.1321C>T MANE Select	ENSP00000261304.2:p.Gln441Ter
NM_000153.3:c.1321C>T	NP_000144.2:p.Gln441Ter
NM_001201401.1:c.1252C>T	NP_001188330.1:p.Gln418Ter
NM_001201401.2:c.1252C>T	NP_001188330.1:p.Gln418Ter
NM_001201402.1:c.1243C>T	NP_001188331.1:p.Gln415Ter
NM_001201402.2:c.1243C>T	NP_001188331.1:p.Gln415Ter
ENST00000261304.6:c.1321C>T	ENSP00000261304.2:p.Gln441Ter
ENST00000393568.8:c.1252C>T	ENSP00000377198.4:p.Gln418Ter
ENST00000393569.6:c.1243C>T	ENSP00000377199.2:p.Gln415Ter
ENST00000544807.6:c.1153C>T	ENSP00000437513.2:p.Gln385Ter
ENST00000555000.5:c.688C>T	ENSP00000450472.1:p.Gln230Ter
ENST00000555179.1:c.38C>T
ENST00000557316.5:c.*719C>T	ENSP00000452314.1:n.*719C>T
XM_011536618.1:c.1153C>T	XP_011534920.1:p.Gln385Ter
XM_011536618.2:c.1153C>T	XP_011534920.1:p.Gln385Ter