Canonical Allele Identifier: CA390753446

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88454861A>T (hg19) ; chr14:g.87988517A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988517A>T , CM000676.2:g.87988517A>T	GRCh38
NC_000014.8:g.88454861A>T , CM000676.1:g.88454861A>T	GRCh37
NC_000014.7:g.87524614A>T	NCBI36
NG_011853.2:g.10047T>A
NG_011853.3:g.10047T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.202T>A MANE Select	ENSP00000261304.2:p.Ser68Thr
ENST00000261304.6:c.202T>A	ENSP00000261304.2:p.Ser68Thr
ENST00000393568.8:c.196-310T>A	ENSP00000377198.4:n.196-310T>A
ENST00000393569.6:c.124T>A	ENSP00000377199.2:p.Ser42Thr
ENST00000474294.6:n.192T>A
ENST00000544807.6:c.34T>A	ENSP00000437513.2:p.Ser12Thr
ENST00000554372.5:c.202T>A	ENSP00000451884.1:p.Ser68Thr
ENST00000554916.5:n.81T>A
ENST00000555956.1:n.7T>A
ENST00000556879.5:c.262T>A	ENSP00000452208.1:n.262T>A
ENST00000557316.5:c.202T>A	ENSP00000452314.1:p.Ser68Thr
ENST00000622264.4:c.192T>A
NM_000153.3:c.202T>A	NP_000144.2:p.Ser68Thr
NM_001201401.1:c.196-310T>A	NP_001188330.1:n.196-310T>A
NM_001201402.1:c.124T>A	NP_001188331.1:p.Ser42Thr
XM_011536618.1:c.34T>A	XP_011534920.1:p.Ser12Thr
XM_011536618.2:c.34T>A	XP_011534920.1:p.Ser12Thr
NM_000153.4:c.202T>A MANE Select	NP_000144.2:p.Ser68Thr
NM_001201401.2:c.196-310T>A	NP_001188330.1:n.196-310T>A
NM_001201402.2:c.124T>A	NP_001188331.1:p.Ser42Thr