Canonical Allele Identifier: CA390745943

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88411897C>G (hg19) ; chr14:g.87945553C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945553C>G , CM000676.2:g.87945553C>G	GRCh38
NC_000014.8:g.88411897C>G , CM000676.1:g.88411897C>G	GRCh37
NC_000014.7:g.87481650C>G	NCBI36
NG_011853.2:g.53011G>C
NG_011853.3:g.53011G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1670G>C MANE Select	ENSP00000261304.2:p.Trp557Ser
ENST00000261304.6:c.1670G>C	ENSP00000261304.2:p.Trp557Ser
ENST00000393568.8:c.1601G>C	ENSP00000377198.4:p.Trp534Ser
ENST00000393569.6:c.1592G>C	ENSP00000377199.2:p.Trp531Ser
ENST00000544807.6:c.1502G>C	ENSP00000437513.2:p.Trp501Ser
ENST00000555000.5:c.1037G>C	ENSP00000450472.1:p.Trp346Ser
ENST00000555179.1:c.206+2175G>C
ENST00000557316.5:c.*1068G>C	ENSP00000452314.1:n.*1068G>C
NM_000153.3:c.1670G>C	NP_000144.2:p.Trp557Ser
NM_001201401.1:c.1601G>C	NP_001188330.1:p.Trp534Ser
NM_001201402.1:c.1592G>C	NP_001188331.1:p.Trp531Ser
XM_011536618.1:c.1502G>C	XP_011534920.1:p.Trp501Ser
XM_011536618.2:c.1502G>C	XP_011534920.1:p.Trp501Ser
NM_000153.4:c.1670G>C MANE Select	NP_000144.2:p.Trp557Ser
NM_001201401.2:c.1601G>C	NP_001188330.1:p.Trp534Ser
NM_001201402.2:c.1592G>C	NP_001188331.1:p.Trp531Ser