Canonical Allele Identifier: CA390749744

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442816A>G (hg19) ; chr14:g.87976472A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976472A>G , CM000676.2:g.87976472A>G	GRCh38
NC_000014.8:g.88442816A>G , CM000676.1:g.88442816A>G	GRCh37
NC_000014.7:g.87512569A>G	NCBI36
NG_011853.2:g.22092T>C
NG_011853.3:g.22092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.638T>C MANE Select	ENSP00000261304.2:p.Leu213Pro
ENST00000261304.6:c.638T>C	ENSP00000261304.2:p.Leu213Pro
ENST00000393568.8:c.569T>C	ENSP00000377198.4:p.Leu190Pro
ENST00000393569.6:c.560T>C	ENSP00000377199.2:p.Leu187Pro
ENST00000474294.6:n.628T>C
ENST00000477716.3:n.393T>C
ENST00000544807.6:c.470T>C	ENSP00000437513.2:p.Leu157Pro
ENST00000554916.5:n.517T>C
ENST00000555000.5:c.5T>C	ENSP00000450472.1:p.Leu2Pro
ENST00000557316.5:c.*36T>C	ENSP00000452314.1:n.*36T>C
ENST00000622264.4:c.628T>C
NM_000153.3:c.638T>C	NP_000144.2:p.Leu213Pro
NM_001201401.1:c.569T>C	NP_001188330.1:p.Leu190Pro
NM_001201402.1:c.560T>C	NP_001188331.1:p.Leu187Pro
XM_011536618.1:c.470T>C	XP_011534920.1:p.Leu157Pro
XM_011536618.2:c.470T>C	XP_011534920.1:p.Leu157Pro
NM_000153.4:c.638T>C MANE Select	NP_000144.2:p.Leu213Pro
NM_001201401.2:c.569T>C	NP_001188330.1:p.Leu190Pro
NM_001201402.2:c.560T>C	NP_001188331.1:p.Leu187Pro