Canonical Allele Identifier: CA390745078

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88401083G>C (hg19) ; chr14:g.87934739G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934739G>C , CM000676.2:g.87934739G>C	GRCh38
NC_000014.8:g.88401083G>C , CM000676.1:g.88401083G>C	GRCh37
NC_000014.7:g.87470836G>C	NCBI36
NG_011853.2:g.63825C>G
NG_011853.3:g.63825C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.2051C>G MANE Select	ENSP00000261304.2:p.Thr684Arg
ENST00000261304.6:c.2051C>G	ENSP00000261304.2:p.Thr684Arg
ENST00000393568.8:c.1982C>G	ENSP00000377198.4:p.Thr661Arg
ENST00000393569.6:c.1973C>G	ENSP00000377199.2:p.Thr658Arg
ENST00000544807.6:c.1744-740C>G	ENSP00000437513.2:n.1744-740C>G
ENST00000555000.5:c.1279-740C>G	ENSP00000450472.1:n.1279-740C>G
NM_000153.3:c.2051C>G	NP_000144.2:p.Thr684Arg
NM_001201401.1:c.1982C>G	NP_001188330.1:p.Thr661Arg
NM_001201402.1:c.1973C>G	NP_001188331.1:p.Thr658Arg
XM_011536618.1:c.1883C>G	XP_011534920.1:p.Thr628Arg
XM_011536618.2:c.1883C>G	XP_011534920.1:p.Thr628Arg
NM_000153.4:c.2051C>G MANE Select	NP_000144.2:p.Thr684Arg
NM_001201401.2:c.1982C>G	NP_001188330.1:p.Thr661Arg
NM_001201402.2:c.1973C>G	NP_001188331.1:p.Thr658Arg