Canonical Allele Identifier: CA390753377

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988483C>G , CM000676.2:g.87988483C>G	GRCh38
NC_000014.8:g.88454827C>G , CM000676.1:g.88454827C>G	GRCh37
NC_000014.7:g.87524580C>G	NCBI36
NG_011853.2:g.10081G>C
NG_011853.3:g.10081G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000153.4:c.236G>C MANE Select	NP_000144.2:p.Arg79Pro
ENST00000261304.7:c.236G>C MANE Select	ENSP00000261304.2:p.Arg79Pro
NM_000153.3:c.236G>C	NP_000144.2:p.Arg79Pro
NM_001201401.1:c.196-276G>C	NP_001188330.1:n.196-276G>C
NM_001201401.2:c.196-276G>C	NP_001188330.1:n.196-276G>C
NM_001201402.1:c.158G>C	NP_001188331.1:p.Arg53Pro
NM_001201402.2:c.158G>C	NP_001188331.1:p.Arg53Pro
ENST00000261304.6:c.236G>C	ENSP00000261304.2:p.Arg79Pro
ENST00000393568.8:c.196-276G>C	ENSP00000377198.4:n.196-276G>C
ENST00000393569.6:c.158G>C	ENSP00000377199.2:p.Arg53Pro
ENST00000474294.6:n.226G>C
ENST00000544807.6:c.68G>C	ENSP00000437513.2:p.Arg23Pro
ENST00000554372.5:c.236G>C	ENSP00000451884.1:p.Arg79Pro
ENST00000554916.5:n.115G>C
ENST00000555956.1:n.41G>C
ENST00000556879.5:c.296G>C	ENSP00000452208.1:n.296G>C
ENST00000557316.5:c.236G>C	ENSP00000452314.1:p.Arg79Pro
ENST00000622264.4:c.226G>C
XM_011536618.1:c.68G>C	XP_011534920.1:p.Arg23Pro
XM_011536618.2:c.68G>C	XP_011534920.1:p.Arg23Pro