Canonical Allele Identifier: CA390747591

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88431939C>A (hg19) ; chr14:g.87965595C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87965595C>A , CM000676.2:g.87965595C>A	GRCh38
NC_000014.8:g.88431939C>A , CM000676.1:g.88431939C>A	GRCh37
NC_000014.7:g.87501692C>A	NCBI36
NG_011853.2:g.32969G>T
NG_011853.3:g.32969G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.943G>T MANE Select	ENSP00000261304.2:p.Glu315Ter
ENST00000261304.6:c.943G>T	ENSP00000261304.2:p.Glu315Ter
ENST00000393568.8:c.874G>T	ENSP00000377198.4:p.Glu292Ter
ENST00000393569.6:c.865G>T	ENSP00000377199.2:p.Glu289Ter
ENST00000474294.6:n.933G>T
ENST00000544807.6:c.775G>T	ENSP00000437513.2:p.Glu259Ter
ENST00000555000.5:c.310G>T	ENSP00000450472.1:p.Glu104Ter
ENST00000557316.5:c.*341G>T	ENSP00000452314.1:n.*341G>T
ENST00000557520.1:n.29G>T
ENST00000622264.4:c.933G>T
NM_000153.3:c.943G>T	NP_000144.2:p.Glu315Ter
NM_001201401.1:c.874G>T	NP_001188330.1:p.Glu292Ter
NM_001201402.1:c.865G>T	NP_001188331.1:p.Glu289Ter
XM_011536618.1:c.775G>T	XP_011534920.1:p.Glu259Ter
XM_011536618.2:c.775G>T	XP_011534920.1:p.Glu259Ter
NM_000153.4:c.943G>T MANE Select	NP_000144.2:p.Glu315Ter
NM_001201401.2:c.874G>T	NP_001188330.1:p.Glu292Ter
NM_001201402.2:c.865G>T	NP_001188331.1:p.Glu289Ter