Canonical Allele Identifier: CA487366429

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88450747A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87984403A>G , CM000676.2:g.87984403A>G	GRCh38
NC_000014.8:g.88450747A>G , CM000676.1:g.88450747A>G	GRCh37
NC_000014.7:g.87520500A>G	NCBI36
NG_011853.2:g.14161T>C
NG_011853.3:g.14161T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.573T>C MANE Select	ENSP00000261304.2:p.Asp191=
ENST00000261304.6:c.573T>C	ENSP00000261304.2:p.Asp191=
ENST00000393568.8:c.504T>C	ENSP00000377198.4:p.Asp168=
ENST00000393569.6:c.495T>C	ENSP00000377199.2:p.Asp165=
ENST00000474294.6:n.563T>C
ENST00000544807.6:c.405T>C	ENSP00000437513.2:p.Asp135=
ENST00000554372.5:c.*322T>C	ENSP00000451884.1:n.*322T>C
ENST00000554916.5:n.452T>C
ENST00000556261.5:n.274T>C
ENST00000557316.5:c.573T>C	ENSP00000452314.1:p.Asp191=
ENST00000622264.4:c.563T>C
NM_000153.3:c.573T>C	NP_000144.2:p.Asp191=
NM_001201401.1:c.504T>C	NP_001188330.1:p.Asp168=
NM_001201402.1:c.495T>C	NP_001188331.1:p.Asp165=
XM_011536618.1:c.405T>C	XP_011534920.1:p.Asp135=
XM_011536618.2:c.405T>C	XP_011534920.1:p.Asp135=
NM_000153.4:c.573T>C MANE Select	NP_000144.2:p.Asp191=
NM_001201401.2:c.504T>C	NP_001188330.1:p.Asp168=
NM_001201402.2:c.495T>C	NP_001188331.1:p.Asp165=