Canonical Allele Identifier: CA390745959

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945559T>C , CM000676.2:g.87945559T>C	GRCh38
NC_000014.8:g.88411903T>C , CM000676.1:g.88411903T>C	GRCh37
NC_000014.7:g.87481656T>C	NCBI36
NG_011853.2:g.53005A>G
NG_011853.3:g.53005A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000153.4:c.1664A>G MANE Select	NP_000144.2:p.Tyr555Cys
ENST00000261304.7:c.1664A>G MANE Select	ENSP00000261304.2:p.Tyr555Cys
NM_000153.3:c.1664A>G	NP_000144.2:p.Tyr555Cys
NM_001201401.1:c.1595A>G	NP_001188330.1:p.Tyr532Cys
NM_001201401.2:c.1595A>G	NP_001188330.1:p.Tyr532Cys
NM_001201402.1:c.1586A>G	NP_001188331.1:p.Tyr529Cys
NM_001201402.2:c.1586A>G	NP_001188331.1:p.Tyr529Cys
ENST00000261304.6:c.1664A>G	ENSP00000261304.2:p.Tyr555Cys
ENST00000393568.8:c.1595A>G	ENSP00000377198.4:p.Tyr532Cys
ENST00000393569.6:c.1586A>G	ENSP00000377199.2:p.Tyr529Cys
ENST00000544807.6:c.1496A>G	ENSP00000437513.2:p.Tyr499Cys
ENST00000555000.5:c.1031A>G	ENSP00000450472.1:p.Tyr344Cys
ENST00000555179.1:c.206+2169A>G
ENST00000557316.5:c.*1062A>G	ENSP00000452314.1:n.*1062A>G
XM_011536618.1:c.1496A>G	XP_011534920.1:p.Tyr499Cys
XM_011536618.2:c.1496A>G	XP_011534920.1:p.Tyr499Cys