Canonical Allele Identifier: CA390746847

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87949913G>A , CM000676.2:g.87949913G>A	GRCh38
NC_000014.8:g.88416257G>A , CM000676.1:g.88416257G>A	GRCh37
NC_000014.7:g.87486010G>A	NCBI36
NG_011853.2:g.48651C>T
NG_011853.3:g.48651C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000153.4:c.1270C>T MANE Select	NP_000144.2:p.Gln424Ter
ENST00000261304.7:c.1270C>T MANE Select	ENSP00000261304.2:p.Gln424Ter
NM_000153.3:c.1270C>T	NP_000144.2:p.Gln424Ter
NM_001201401.1:c.1201C>T	NP_001188330.1:p.Gln401Ter
NM_001201401.2:c.1201C>T	NP_001188330.1:p.Gln401Ter
NM_001201402.1:c.1192C>T	NP_001188331.1:p.Gln398Ter
NM_001201402.2:c.1192C>T	NP_001188331.1:p.Gln398Ter
ENST00000261304.6:c.1270C>T	ENSP00000261304.2:p.Gln424Ter
ENST00000393568.8:c.1201C>T	ENSP00000377198.4:p.Gln401Ter
ENST00000393569.6:c.1192C>T	ENSP00000377199.2:p.Gln398Ter
ENST00000544807.6:c.1102C>T	ENSP00000437513.2:p.Gln368Ter
ENST00000555000.5:c.637C>T	ENSP00000450472.1:p.Gln213Ter
ENST00000557316.5:c.*668C>T	ENSP00000452314.1:n.*668C>T
XM_011536618.1:c.1102C>T	XP_011534920.1:p.Gln368Ter
XM_011536618.2:c.1102C>T	XP_011534920.1:p.Gln368Ter