Canonical Allele Identifier: CA487366423

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88450738T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87984394T>A , CM000676.2:g.87984394T>A	GRCh38
NC_000014.8:g.88450738T>A , CM000676.1:g.88450738T>A	GRCh37
NC_000014.7:g.87520491T>A	NCBI36
NG_011853.2:g.14170A>T
NG_011853.3:g.14170A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.582A>T MANE Select	ENSP00000261304.2:p.Gly194=
ENST00000261304.6:c.582A>T	ENSP00000261304.2:p.Gly194=
ENST00000393568.8:c.513A>T	ENSP00000377198.4:p.Gly171=
ENST00000393569.6:c.504A>T	ENSP00000377199.2:p.Gly168=
ENST00000474294.6:n.572A>T
ENST00000544807.6:c.414A>T	ENSP00000437513.2:p.Gly138=
ENST00000554372.5:c.*331A>T	ENSP00000451884.1:n.*331A>T
ENST00000554916.5:n.461A>T
ENST00000556261.5:n.283A>T
ENST00000557316.5:c.582A>T	ENSP00000452314.1:p.Gly194=
ENST00000622264.4:c.572A>T
NM_000153.3:c.582A>T	NP_000144.2:p.Gly194=
NM_001201401.1:c.513A>T	NP_001188330.1:p.Gly171=
NM_001201402.1:c.504A>T	NP_001188331.1:p.Gly168=
XM_011536618.1:c.414A>T	XP_011534920.1:p.Gly138=
XM_011536618.2:c.414A>T	XP_011534920.1:p.Gly138=
NM_000153.4:c.582A>T MANE Select	NP_000144.2:p.Gly194=
NM_001201401.2:c.513A>T	NP_001188330.1:p.Gly171=
NM_001201402.2:c.504A>T	NP_001188331.1:p.Gly168=