Canonical Allele Identifier: CA390745650

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88407774A>G (hg19) ; chr14:g.87941430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87941430A>G , CM000676.2:g.87941430A>G	GRCh38
NC_000014.8:g.88407774A>G , CM000676.1:g.88407774A>G	GRCh37
NC_000014.7:g.87477527A>G	NCBI36
NG_011853.2:g.57134T>C
NG_011853.3:g.57134T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1799T>C MANE Select	ENSP00000261304.2:p.Phe600Ser
ENST00000261304.6:c.1799T>C	ENSP00000261304.2:p.Phe600Ser
ENST00000393568.8:c.1730T>C	ENSP00000377198.4:p.Phe577Ser
ENST00000393569.6:c.1721T>C	ENSP00000377199.2:p.Phe574Ser
ENST00000544807.6:c.1631T>C	ENSP00000437513.2:p.Phe544Ser
ENST00000555000.5:c.1166T>C	ENSP00000450472.1:p.Phe389Ser
ENST00000555179.1:c.335T>C
ENST00000557316.5:c.*1197T>C	ENSP00000452314.1:n.*1197T>C
NM_000153.3:c.1799T>C	NP_000144.2:p.Phe600Ser
NM_001201401.1:c.1730T>C	NP_001188330.1:p.Phe577Ser
NM_001201402.1:c.1721T>C	NP_001188331.1:p.Phe574Ser
XM_011536618.1:c.1631T>C	XP_011534920.1:p.Phe544Ser
XM_011536618.2:c.1631T>C	XP_011534920.1:p.Phe544Ser
NM_000153.4:c.1799T>C MANE Select	NP_000144.2:p.Phe600Ser
NM_001201401.2:c.1730T>C	NP_001188330.1:p.Phe577Ser
NM_001201402.2:c.1721T>C	NP_001188331.1:p.Phe574Ser