Canonical Allele Identifier: CA390746373

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414077T>A (hg19) ; chr14:g.87947733T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947733T>A , CM000676.2:g.87947733T>A	GRCh38
NC_000014.8:g.88414077T>A , CM000676.1:g.88414077T>A	GRCh37
NC_000014.7:g.87483830T>A	NCBI36
NG_011853.2:g.50831A>T
NG_011853.3:g.50831A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1484A>T MANE Select	ENSP00000261304.2:p.Asn495Ile
ENST00000261304.6:c.1484A>T	ENSP00000261304.2:p.Asn495Ile
ENST00000393568.8:c.1415A>T	ENSP00000377198.4:p.Asn472Ile
ENST00000393569.6:c.1406A>T	ENSP00000377199.2:p.Asn469Ile
ENST00000544807.6:c.1316A>T	ENSP00000437513.2:p.Asn439Ile
ENST00000555000.5:c.851A>T	ENSP00000450472.1:p.Asn284Ile
ENST00000555179.1:c.201A>T
ENST00000557316.5:c.*882A>T	ENSP00000452314.1:n.*882A>T
NM_000153.3:c.1484A>T	NP_000144.2:p.Asn495Ile
NM_001201401.1:c.1415A>T	NP_001188330.1:p.Asn472Ile
NM_001201402.1:c.1406A>T	NP_001188331.1:p.Asn469Ile
XM_011536618.1:c.1316A>T	XP_011534920.1:p.Asn439Ile
XM_011536618.2:c.1316A>T	XP_011534920.1:p.Asn439Ile
NM_000153.4:c.1484A>T MANE Select	NP_000144.2:p.Asn495Ile
NM_001201401.2:c.1415A>T	NP_001188330.1:p.Asn472Ile
NM_001201402.2:c.1406A>T	NP_001188331.1:p.Asn469Ile