Canonical Allele Identifier: CA2153352671

Gene: GALC

Linked Data

• dbSNP Id: rs1884761427
• gnomAD v4: 14-87939884-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87939884A>T , CM000676.2:g.87939884A>T	GRCh38
NC_000014.8:g.88406228A>T , CM000676.1:g.88406228A>T	GRCh37
NC_000014.7:g.87475981A>T	NCBI36
NG_011853.2:g.58680T>A
NG_011853.3:g.58680T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1911+21T>A MANE Select	ENSP00000261304.2:n.1911+21T>A
ENST00000261304.6:c.1911+21T>A	ENSP00000261304.2:n.1911+21T>A
ENST00000393568.8:c.1842+21T>A	ENSP00000377198.4:n.1842+21T>A
ENST00000393569.6:c.1833+21T>A	ENSP00000377199.2:n.1833+21T>A
ENST00000544807.6:c.1743+21T>A	ENSP00000437513.2:n.1743+21T>A
ENST00000555000.5:c.1278+21T>A	ENSP00000450472.1:n.1278+21T>A
ENST00000555179.1:c.447+21T>A
NM_000153.3:c.1911+21T>A	NP_000144.2:n.1911+21T>A
NM_001201401.1:c.1842+21T>A	NP_001188330.1:n.1842+21T>A
NM_001201402.1:c.1833+21T>A	NP_001188331.1:n.1833+21T>A
XM_011536618.1:c.1743+21T>A	XP_011534920.1:n.1743+21T>A
XM_011536618.2:c.1743+21T>A	XP_011534920.1:n.1743+21T>A
NM_000153.4:c.1911+21T>A MANE Select	NP_000144.2:n.1911+21T>A
NM_001201401.2:c.1842+21T>A	NP_001188330.1:n.1842+21T>A
NM_001201402.2:c.1833+21T>A	NP_001188331.1:n.1833+21T>A