Canonical Allele Identifier: CA487354490

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88401091C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934747C>A , CM000676.2:g.87934747C>A	GRCh38
NC_000014.8:g.88401091C>A , CM000676.1:g.88401091C>A	GRCh37
NC_000014.7:g.87470844C>A	NCBI36
NG_011853.2:g.63817G>T
NG_011853.3:g.63817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.2043G>T MANE Select	ENSP00000261304.2:p.Val681=
ENST00000261304.6:c.2043G>T	ENSP00000261304.2:p.Val681=
ENST00000393568.8:c.1974G>T	ENSP00000377198.4:p.Val658=
ENST00000393569.6:c.1965G>T	ENSP00000377199.2:p.Val655=
ENST00000544807.6:c.1744-748G>T	ENSP00000437513.2:n.1744-748G>T
ENST00000555000.5:c.1279-748G>T	ENSP00000450472.1:n.1279-748G>T
NM_000153.3:c.2043G>T	NP_000144.2:p.Val681=
NM_001201401.1:c.1974G>T	NP_001188330.1:p.Val658=
NM_001201402.1:c.1965G>T	NP_001188331.1:p.Val655=
XM_011536618.1:c.1875G>T	XP_011534920.1:p.Val625=
XM_011536618.2:c.1875G>T	XP_011534920.1:p.Val625=
NM_000153.4:c.2043G>T MANE Select	NP_000144.2:p.Val681=
NM_001201401.2:c.1974G>T	NP_001188330.1:p.Val658=
NM_001201402.2:c.1965G>T	NP_001188331.1:p.Val655=