Canonical Allele Identifier: CA390746313

Gene: GALC

Linked Data

• dbSNP Id: rs1347431324
• gnomAD v2: 14-88412063-T-C
• gnomAD v3: 14-87945719-T-C
• gnomAD v4: 14-87945719-T-C
• MyVariant Identifiers: chr14:g.88412063T>C (hg19) ; chr14:g.87945719T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945719T>C , CM000676.2:g.87945719T>C	GRCh38
NC_000014.8:g.88412063T>C , CM000676.1:g.88412063T>C	GRCh37
NC_000014.7:g.87481816T>C	NCBI36
NG_011853.2:g.52845A>G
NG_011853.3:g.52845A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1504A>G MANE Select	ENSP00000261304.2:p.Ser502Gly
ENST00000261304.6:c.1504A>G	ENSP00000261304.2:p.Ser502Gly
ENST00000393568.8:c.1435A>G	ENSP00000377198.4:p.Ser479Gly
ENST00000393569.6:c.1426A>G	ENSP00000377199.2:p.Ser476Gly
ENST00000544807.6:c.1336A>G	ENSP00000437513.2:p.Ser446Gly
ENST00000555000.5:c.871A>G	ENSP00000450472.1:p.Ser291Gly
ENST00000555179.1:c.206+2009A>G
ENST00000557316.5:c.*902A>G	ENSP00000452314.1:n.*902A>G
NM_000153.3:c.1504A>G	NP_000144.2:p.Ser502Gly
NM_001201401.1:c.1435A>G	NP_001188330.1:p.Ser479Gly
NM_001201402.1:c.1426A>G	NP_001188331.1:p.Ser476Gly
XM_011536618.1:c.1336A>G	XP_011534920.1:p.Ser446Gly
XM_011536618.2:c.1336A>G	XP_011534920.1:p.Ser446Gly
NM_000153.4:c.1504A>G MANE Select	NP_000144.2:p.Ser502Gly
NM_001201401.2:c.1435A>G	NP_001188330.1:p.Ser479Gly
NM_001201402.2:c.1426A>G	NP_001188331.1:p.Ser476Gly