Canonical Allele Identifier: CA390749326

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442723A>T (hg19) ; chr14:g.87976379A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976379A>T , CM000676.2:g.87976379A>T	GRCh38
NC_000014.8:g.88442723A>T , CM000676.1:g.88442723A>T	GRCh37
NC_000014.7:g.87512476A>T	NCBI36
NG_011853.2:g.22185T>A
NG_011853.3:g.22185T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.731T>A MANE Select	ENSP00000261304.2:p.Phe244Tyr
ENST00000261304.6:c.731T>A	ENSP00000261304.2:p.Phe244Tyr
ENST00000393568.8:c.662T>A	ENSP00000377198.4:p.Phe221Tyr
ENST00000393569.6:c.653T>A	ENSP00000377199.2:p.Phe218Tyr
ENST00000474294.6:n.721T>A
ENST00000477716.3:n.486T>A
ENST00000544807.6:c.563T>A	ENSP00000437513.2:p.Phe188Tyr
ENST00000554916.5:n.610T>A
ENST00000555000.5:c.98T>A	ENSP00000450472.1:p.Phe33Tyr
ENST00000557316.5:c.*129T>A	ENSP00000452314.1:n.*129T>A
ENST00000622264.4:c.721T>A
NM_000153.3:c.731T>A	NP_000144.2:p.Phe244Tyr
NM_001201401.1:c.662T>A	NP_001188330.1:p.Phe221Tyr
NM_001201402.1:c.653T>A	NP_001188331.1:p.Phe218Tyr
XM_011536618.1:c.563T>A	XP_011534920.1:p.Phe188Tyr
XM_011536618.2:c.563T>A	XP_011534920.1:p.Phe188Tyr
NM_000153.4:c.731T>A MANE Select	NP_000144.2:p.Phe244Tyr
NM_001201401.2:c.662T>A	NP_001188330.1:p.Phe221Tyr
NM_001201402.2:c.653T>A	NP_001188331.1:p.Phe218Tyr