Canonical Allele Identifier: CA264711042

Gene: GALC

Linked Data

• dbSNP Id: rs1057168230
• gnomAD v2: 14-88450633-C-T
• gnomAD v3: 14-87984289-C-T
• gnomAD v4: 14-87984289-C-T
• MyVariant Identifiers: chr14:g.88450633C>T (hg19) ; chr14:g.87984289C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87984289C>T , CM000676.2:g.87984289C>T	GRCh38
NC_000014.8:g.88450633C>T , CM000676.1:g.88450633C>T	GRCh37
NC_000014.7:g.87520386C>T	NCBI36
NG_011853.2:g.14275G>A
NG_011853.3:g.14275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.582+105G>A MANE Select	ENSP00000261304.2:n.582+105G>A
ENST00000261304.6:c.582+105G>A	ENSP00000261304.2:n.582+105G>A
ENST00000393568.8:c.513+105G>A	ENSP00000377198.4:n.513+105G>A
ENST00000393569.6:c.504+105G>A	ENSP00000377199.2:n.504+105G>A
ENST00000474294.6:n.572+105G>A
ENST00000544807.6:c.414+105G>A	ENSP00000437513.2:n.414+105G>A
ENST00000554372.5:c.*331+105G>A	ENSP00000451884.1:n.*331+105G>A
ENST00000554916.5:n.461+105G>A
ENST00000556261.5:n.283+105G>A
ENST00000557316.5:c.582+105G>A	ENSP00000452314.1:n.582+105G>A
ENST00000622264.4:c.572+105G>A
NM_000153.3:c.582+105G>A	NP_000144.2:n.582+105G>A
NM_001201401.1:c.513+105G>A	NP_001188330.1:n.513+105G>A
NM_001201402.1:c.504+105G>A	NP_001188331.1:n.504+105G>A
XM_011536618.1:c.414+105G>A	XP_011534920.1:n.414+105G>A
XM_011536618.2:c.414+105G>A	XP_011534920.1:n.414+105G>A
NM_000153.4:c.582+105G>A MANE Select	NP_000144.2:n.582+105G>A
NM_001201401.2:c.513+105G>A	NP_001188330.1:n.513+105G>A
NM_001201402.2:c.504+105G>A	NP_001188331.1:n.504+105G>A