Canonical Allele Identifier: CA7297067

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87949911C>T , CM000676.2:g.87949911C>T	GRCh38
NC_000014.8:g.88416255C>T , CM000676.1:g.88416255C>T	GRCh37
NC_000014.7:g.87486008C>T	NCBI36
NG_011853.2:g.48653G>A
NG_011853.3:g.48653G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000153.4:c.1272G>A MANE Select	NP_000144.2:p.Gln424=
ENST00000261304.7:c.1272G>A MANE Select	ENSP00000261304.2:p.Gln424=
NM_000153.3:c.1272G>A	NP_000144.2:p.Gln424=
NM_001201401.1:c.1203G>A	NP_001188330.1:p.Gln401=
NM_001201401.2:c.1203G>A	NP_001188330.1:p.Gln401=
NM_001201402.1:c.1194G>A	NP_001188331.1:p.Gln398=
NM_001201402.2:c.1194G>A	NP_001188331.1:p.Gln398=
ENST00000261304.6:c.1272G>A	ENSP00000261304.2:p.Gln424=
ENST00000393568.8:c.1203G>A	ENSP00000377198.4:p.Gln401=
ENST00000393569.6:c.1194G>A	ENSP00000377199.2:p.Gln398=
ENST00000544807.6:c.1104G>A	ENSP00000437513.2:p.Gln368=
ENST00000555000.5:c.639G>A	ENSP00000450472.1:p.Gln213=
ENST00000557316.5:c.*670G>A	ENSP00000452314.1:n.*670G>A
XM_011536618.1:c.1104G>A	XP_011534920.1:p.Gln368=
XM_011536618.2:c.1104G>A	XP_011534920.1:p.Gln368=