Canonical Allele Identifier: CA487366732

Gene: GALC

Linked Data

• dbSNP Id: rs1375871159
• gnomAD v3: 14-87988521-T-C
• gnomAD v4: 14-87988521-T-C
• MyVariant Identifiers: chr14:g.88454865T>C (hg19) ; chr14:g.87988521T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988521T>C , CM000676.2:g.87988521T>C	GRCh38
NC_000014.8:g.88454865T>C , CM000676.1:g.88454865T>C	GRCh37
NC_000014.7:g.87524618T>C	NCBI36
NG_011853.2:g.10043A>G
NG_011853.3:g.10043A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.198A>G MANE Select	ENSP00000261304.2:p.Ala66=
ENST00000261304.6:c.198A>G	ENSP00000261304.2:p.Ala66=
ENST00000393568.8:c.196-314A>G	ENSP00000377198.4:n.196-314A>G
ENST00000393569.6:c.120A>G	ENSP00000377199.2:p.Ala40=
ENST00000474294.6:n.188A>G
ENST00000544807.6:c.30A>G	ENSP00000437513.2:p.Ala10=
ENST00000554372.5:c.198A>G	ENSP00000451884.1:p.Ala66=
ENST00000554916.5:n.77A>G
ENST00000555956.1:n.3A>G
ENST00000556879.5:c.258A>G	ENSP00000452208.1:n.258A>G
ENST00000557316.5:c.198A>G	ENSP00000452314.1:p.Ala66=
ENST00000622264.4:c.188A>G
NM_000153.3:c.198A>G	NP_000144.2:p.Ala66=
NM_001201401.1:c.196-314A>G	NP_001188330.1:n.196-314A>G
NM_001201402.1:c.120A>G	NP_001188331.1:p.Ala40=
XM_011536618.1:c.30A>G	XP_011534920.1:p.Ala10=
XM_011536618.2:c.30A>G	XP_011534920.1:p.Ala10=
NM_000153.4:c.198A>G MANE Select	NP_000144.2:p.Ala66=
NM_001201401.2:c.196-314A>G	NP_001188330.1:n.196-314A>G
NM_001201402.2:c.120A>G	NP_001188331.1:p.Ala40=