Canonical Allele Identifier: CA390745098

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88401093C>G (hg19) ; chr14:g.87934749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934749C>G , CM000676.2:g.87934749C>G	GRCh38
NC_000014.8:g.88401093C>G , CM000676.1:g.88401093C>G	GRCh37
NC_000014.7:g.87470846C>G	NCBI36
NG_011853.2:g.63815G>C
NG_011853.3:g.63815G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.2041G>C MANE Select	ENSP00000261304.2:p.Val681Leu
ENST00000261304.6:c.2041G>C	ENSP00000261304.2:p.Val681Leu
ENST00000393568.8:c.1972G>C	ENSP00000377198.4:p.Val658Leu
ENST00000393569.6:c.1963G>C	ENSP00000377199.2:p.Val655Leu
ENST00000544807.6:c.1744-750G>C	ENSP00000437513.2:n.1744-750G>C
ENST00000555000.5:c.1279-750G>C	ENSP00000450472.1:n.1279-750G>C
NM_000153.3:c.2041G>C	NP_000144.2:p.Val681Leu
NM_001201401.1:c.1972G>C	NP_001188330.1:p.Val658Leu
NM_001201402.1:c.1963G>C	NP_001188331.1:p.Val655Leu
XM_011536618.1:c.1873G>C	XP_011534920.1:p.Val625Leu
XM_011536618.2:c.1873G>C	XP_011534920.1:p.Val625Leu
NM_000153.4:c.2041G>C MANE Select	NP_000144.2:p.Val681Leu
NM_001201401.2:c.1972G>C	NP_001188330.1:p.Val658Leu
NM_001201402.2:c.1963G>C	NP_001188331.1:p.Val655Leu