Canonical Allele Identifier: CA2625960683

Gene: GALC

Linked Data

• gnomAD v4: 14-87976930-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976930C>A , CM000676.2:g.87976930C>A	GRCh38
NC_000014.8:g.88443274C>A , CM000676.1:g.88443274C>A	GRCh37
NC_000014.7:g.87513027C>A	NCBI36
NG_011853.2:g.21634G>T
NG_011853.3:g.21634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.622-442G>T MANE Select	ENSP00000261304.2:n.622-442G>T
ENST00000261304.6:c.622-442G>T	ENSP00000261304.2:n.622-442G>T
ENST00000393568.8:c.553-442G>T	ENSP00000377198.4:n.553-442G>T
ENST00000393569.6:c.544-442G>T	ENSP00000377199.2:n.544-442G>T
ENST00000474294.6:n.612-442G>T
ENST00000544807.6:c.454-442G>T	ENSP00000437513.2:n.454-442G>T
ENST00000554916.5:n.501-442G>T
ENST00000555000.5:c.-12-442G>T	ENSP00000450472.1:n.-12-442G>T
ENST00000557316.5:c.*20-442G>T	ENSP00000452314.1:n.*20-442G>T
ENST00000622264.4:c.612-442G>T
NM_000153.3:c.622-442G>T	NP_000144.2:n.622-442G>T
NM_001201401.1:c.553-442G>T	NP_001188330.1:n.553-442G>T
NM_001201402.1:c.544-442G>T	NP_001188331.1:n.544-442G>T
XM_011536618.1:c.454-442G>T	XP_011534920.1:n.454-442G>T
XM_011536618.2:c.454-442G>T	XP_011534920.1:n.454-442G>T
NM_000153.4:c.622-442G>T MANE Select	NP_000144.2:n.622-442G>T
NM_001201401.2:c.553-442G>T	NP_001188330.1:n.553-442G>T
NM_001201402.2:c.544-442G>T	NP_001188331.1:n.544-442G>T