Canonical Allele Identifier: CA487354472

Gene: GALC

Linked Data

• gnomAD v4: 14-87934741-G-C
• MyVariant Identifiers: chr14:g.88401085G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934741G>C , CM000676.2:g.87934741G>C	GRCh38
NC_000014.8:g.88401085G>C , CM000676.1:g.88401085G>C	GRCh37
NC_000014.7:g.87470838G>C	NCBI36
NG_011853.2:g.63823C>G
NG_011853.3:g.63823C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.2049C>G MANE Select	ENSP00000261304.2:p.Ala683=
ENST00000261304.6:c.2049C>G	ENSP00000261304.2:p.Ala683=
ENST00000393568.8:c.1980C>G	ENSP00000377198.4:p.Ala660=
ENST00000393569.6:c.1971C>G	ENSP00000377199.2:p.Ala657=
ENST00000544807.6:c.1744-742C>G	ENSP00000437513.2:n.1744-742C>G
ENST00000555000.5:c.1279-742C>G	ENSP00000450472.1:n.1279-742C>G
NM_000153.3:c.2049C>G	NP_000144.2:p.Ala683=
NM_001201401.1:c.1980C>G	NP_001188330.1:p.Ala660=
NM_001201402.1:c.1971C>G	NP_001188331.1:p.Ala657=
XM_011536618.1:c.1881C>G	XP_011534920.1:p.Ala627=
XM_011536618.2:c.1881C>G	XP_011534920.1:p.Ala627=
NM_000153.4:c.2049C>G MANE Select	NP_000144.2:p.Ala683=
NM_001201401.2:c.1980C>G	NP_001188330.1:p.Ala660=
NM_001201402.2:c.1971C>G	NP_001188331.1:p.Ala657=