Canonical Allele Identifier: CA2625958947

Gene: GALC

Linked Data

• gnomAD v4: 14-87934661-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934661G>T , CM000676.2:g.87934661G>T	GRCh38
NC_000014.8:g.88401005G>T , CM000676.1:g.88401005G>T	GRCh37
NC_000014.7:g.87470758G>T	NCBI36
NG_011853.2:g.63903C>A
NG_011853.3:g.63903C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.*71C>A MANE Select	ENSP00000261304.2:n.*71C>A
ENST00000261304.6:c.*71C>A	ENSP00000261304.2:n.*71C>A
ENST00000393569.6:c.*71C>A	ENSP00000377199.2:n.*71C>A
ENST00000544807.6:c.1744-662C>A	ENSP00000437513.2:n.1744-662C>A
ENST00000555000.5:c.1279-662C>A	ENSP00000450472.1:n.1279-662C>A
NM_000153.3:c.*71C>A	NP_000144.2:n.*71C>A
NM_001201401.1:c.*71C>A	NP_001188330.1:n.*71C>A
NM_001201402.1:c.*71C>A	NP_001188331.1:n.*71C>A
XM_011536618.1:c.*71C>A	XP_011534920.1:n.*71C>A
XM_011536618.2:c.*71C>A	XP_011534920.1:n.*71C>A
NM_000153.4:c.*71C>A MANE Select	NP_000144.2:n.*71C>A
NM_001201401.2:c.*71C>A	NP_001188330.1:n.*71C>A
NM_001201402.2:c.*71C>A	NP_001188331.1:n.*71C>A