Canonical Allele Identifier: CA709650958

Gene: GALC

Linked Data

• dbSNP Id: rs1335916759
• MyVariant Identifiers: chr14:g.88413915_88413916insA (hg19) ; chr14:g.87947571_87947572insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947577dup , CM000676.2:g.87947577dup	GRCh38
NC_000014.8:g.88413921dup , CM000676.1:g.88413921dup	GRCh37
NC_000014.7:g.87483674dup	NCBI36
NG_011853.2:g.50992dup
NG_011853.3:g.50992dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1489+156dup MANE Select	ENSP00000261304.2:n.1489+156dup
ENST00000261304.6:c.1489+156dup	ENSP00000261304.2:n.1489+156dup
ENST00000393568.8:c.1420+156dup	ENSP00000377198.4:n.1420+156dup
ENST00000393569.6:c.1411+156dup	ENSP00000377199.2:n.1411+156dup
ENST00000544807.6:c.1321+156dup	ENSP00000437513.2:n.1321+156dup
ENST00000555000.5:c.856+156dup	ENSP00000450472.1:n.856+156dup
ENST00000555179.1:c.206+156dup
ENST00000557316.5:c.*887+156dup	ENSP00000452314.1:n.*887+156dup
NM_000153.3:c.1489+156dup	NP_000144.2:n.1489+156dup
NM_001201401.1:c.1420+156dup	NP_001188330.1:n.1420+156dup
NM_001201402.1:c.1411+156dup	NP_001188331.1:n.1411+156dup
XM_011536618.1:c.1321+156dup	XP_011534920.1:n.1321+156dup
XM_011536618.2:c.1321+156dup	XP_011534920.1:n.1321+156dup
NM_000153.4:c.1489+156dup MANE Select	NP_000144.2:n.1489+156dup
NM_001201401.2:c.1420+156dup	NP_001188330.1:n.1420+156dup
NM_001201402.2:c.1411+156dup	NP_001188331.1:n.1411+156dup