Canonical Allele Identifier: CA487366286

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442782T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976438T>G , CM000676.2:g.87976438T>G	GRCh38
NC_000014.8:g.88442782T>G , CM000676.1:g.88442782T>G	GRCh37
NC_000014.7:g.87512535T>G	NCBI36
NG_011853.2:g.22126A>C
NG_011853.3:g.22126A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.672A>C MANE Select	ENSP00000261304.2:p.Ile224=
ENST00000261304.6:c.672A>C	ENSP00000261304.2:p.Ile224=
ENST00000393568.8:c.603A>C	ENSP00000377198.4:p.Ile201=
ENST00000393569.6:c.594A>C	ENSP00000377199.2:p.Ile198=
ENST00000474294.6:n.662A>C
ENST00000477716.3:n.427A>C
ENST00000544807.6:c.504A>C	ENSP00000437513.2:p.Ile168=
ENST00000554916.5:n.551A>C
ENST00000555000.5:c.39A>C	ENSP00000450472.1:p.Ile13=
ENST00000557316.5:c.*70A>C	ENSP00000452314.1:n.*70A>C
ENST00000622264.4:c.662A>C
NM_000153.3:c.672A>C	NP_000144.2:p.Ile224=
NM_001201401.1:c.603A>C	NP_001188330.1:p.Ile201=
NM_001201402.1:c.594A>C	NP_001188331.1:p.Ile198=
XM_011536618.1:c.504A>C	XP_011534920.1:p.Ile168=
XM_011536618.2:c.504A>C	XP_011534920.1:p.Ile168=
NM_000153.4:c.672A>C MANE Select	NP_000144.2:p.Ile224=
NM_001201401.2:c.603A>C	NP_001188330.1:p.Ile201=
NM_001201402.2:c.594A>C	NP_001188331.1:p.Ile198=