Canonical Allele Identifier: CA390746629

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414198T>A (hg19) ; chr14:g.87947854T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947854T>A , CM000676.2:g.87947854T>A	GRCh38
NC_000014.8:g.88414198T>A , CM000676.1:g.88414198T>A	GRCh37
NC_000014.7:g.87483951T>A	NCBI36
NG_011853.2:g.50710A>T
NG_011853.3:g.50710A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1363A>T MANE Select	ENSP00000261304.2:p.Thr455Ser
ENST00000261304.6:c.1363A>T	ENSP00000261304.2:p.Thr455Ser
ENST00000393568.8:c.1294A>T	ENSP00000377198.4:p.Thr432Ser
ENST00000393569.6:c.1285A>T	ENSP00000377199.2:p.Thr429Ser
ENST00000544807.6:c.1195A>T	ENSP00000437513.2:p.Thr399Ser
ENST00000555000.5:c.730A>T	ENSP00000450472.1:p.Thr244Ser
ENST00000555179.1:c.80A>T
ENST00000557316.5:c.*761A>T	ENSP00000452314.1:n.*761A>T
NM_000153.3:c.1363A>T	NP_000144.2:p.Thr455Ser
NM_001201401.1:c.1294A>T	NP_001188330.1:p.Thr432Ser
NM_001201402.1:c.1285A>T	NP_001188331.1:p.Thr429Ser
XM_011536618.1:c.1195A>T	XP_011534920.1:p.Thr399Ser
XM_011536618.2:c.1195A>T	XP_011534920.1:p.Thr399Ser
NM_000153.4:c.1363A>T MANE Select	NP_000144.2:p.Thr455Ser
NM_001201401.2:c.1294A>T	NP_001188330.1:p.Thr432Ser
NM_001201402.2:c.1285A>T	NP_001188331.1:p.Thr429Ser