Canonical Allele Identifier: CA487366727

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88454859G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988515G>T , CM000676.2:g.87988515G>T	GRCh38
NC_000014.8:g.88454859G>T , CM000676.1:g.88454859G>T	GRCh37
NC_000014.7:g.87524612G>T	NCBI36
NG_011853.2:g.10049C>A
NG_011853.3:g.10049C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.204C>A MANE Select	ENSP00000261304.2:p.Ser68=
ENST00000261304.6:c.204C>A	ENSP00000261304.2:p.Ser68=
ENST00000393568.8:c.196-308C>A	ENSP00000377198.4:n.196-308C>A
ENST00000393569.6:c.126C>A	ENSP00000377199.2:p.Ser42=
ENST00000474294.6:n.194C>A
ENST00000544807.6:c.36C>A	ENSP00000437513.2:p.Ser12=
ENST00000554372.5:c.204C>A	ENSP00000451884.1:p.Ser68=
ENST00000554916.5:n.83C>A
ENST00000555956.1:n.9C>A
ENST00000556879.5:c.264C>A	ENSP00000452208.1:n.264C>A
ENST00000557316.5:c.204C>A	ENSP00000452314.1:p.Ser68=
ENST00000622264.4:c.194C>A
NM_000153.3:c.204C>A	NP_000144.2:p.Ser68=
NM_001201401.1:c.196-308C>A	NP_001188330.1:n.196-308C>A
NM_001201402.1:c.126C>A	NP_001188331.1:p.Ser42=
XM_011536618.1:c.36C>A	XP_011534920.1:p.Ser12=
XM_011536618.2:c.36C>A	XP_011534920.1:p.Ser12=
NM_000153.4:c.204C>A MANE Select	NP_000144.2:p.Ser68=
NM_001201401.2:c.196-308C>A	NP_001188330.1:n.196-308C>A
NM_001201402.2:c.126C>A	NP_001188331.1:p.Ser42=