Canonical Allele Identifier: CA487355619

Gene: GALC

Linked Data

• gnomAD v4: 14-87947759-G-A
• MyVariant Identifiers: chr14:g.88414103G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947759G>A , CM000676.2:g.87947759G>A	GRCh38
NC_000014.8:g.88414103G>A , CM000676.1:g.88414103G>A	GRCh37
NC_000014.7:g.87483856G>A	NCBI36
NG_011853.2:g.50805C>T
NG_011853.3:g.50805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1458C>T MANE Select	ENSP00000261304.2:p.Phe486=
ENST00000261304.6:c.1458C>T	ENSP00000261304.2:p.Phe486=
ENST00000393568.8:c.1389C>T	ENSP00000377198.4:p.Phe463=
ENST00000393569.6:c.1380C>T	ENSP00000377199.2:p.Phe460=
ENST00000544807.6:c.1290C>T	ENSP00000437513.2:p.Phe430=
ENST00000555000.5:c.825C>T	ENSP00000450472.1:p.Phe275=
ENST00000555179.1:c.175C>T
ENST00000557316.5:c.*856C>T	ENSP00000452314.1:n.*856C>T
NM_000153.3:c.1458C>T	NP_000144.2:p.Phe486=
NM_001201401.1:c.1389C>T	NP_001188330.1:p.Phe463=
NM_001201402.1:c.1380C>T	NP_001188331.1:p.Phe460=
XM_011536618.1:c.1290C>T	XP_011534920.1:p.Phe430=
XM_011536618.2:c.1290C>T	XP_011534920.1:p.Phe430=
NM_000153.4:c.1458C>T MANE Select	NP_000144.2:p.Phe486=
NM_001201401.2:c.1389C>T	NP_001188330.1:p.Phe463=
NM_001201402.2:c.1380C>T	NP_001188331.1:p.Phe460=