Canonical Allele Identifier: CA390746336

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88412072G>A (hg19) ; chr14:g.87945728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945728G>A , CM000676.2:g.87945728G>A	GRCh38
NC_000014.8:g.88412072G>A , CM000676.1:g.88412072G>A	GRCh37
NC_000014.7:g.87481825G>A	NCBI36
NG_011853.2:g.52836C>T
NG_011853.3:g.52836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1495C>T MANE Select	ENSP00000261304.2:p.Pro499Ser
ENST00000261304.6:c.1495C>T	ENSP00000261304.2:p.Pro499Ser
ENST00000393568.8:c.1426C>T	ENSP00000377198.4:p.Pro476Ser
ENST00000393569.6:c.1417C>T	ENSP00000377199.2:p.Pro473Ser
ENST00000544807.6:c.1327C>T	ENSP00000437513.2:p.Pro443Ser
ENST00000555000.5:c.862C>T	ENSP00000450472.1:p.Pro288Ser
ENST00000555179.1:c.206+2000C>T
ENST00000557316.5:c.*893C>T	ENSP00000452314.1:n.*893C>T
NM_000153.3:c.1495C>T	NP_000144.2:p.Pro499Ser
NM_001201401.1:c.1426C>T	NP_001188330.1:p.Pro476Ser
NM_001201402.1:c.1417C>T	NP_001188331.1:p.Pro473Ser
XM_011536618.1:c.1327C>T	XP_011534920.1:p.Pro443Ser
XM_011536618.2:c.1327C>T	XP_011534920.1:p.Pro443Ser
NM_000153.4:c.1495C>T MANE Select	NP_000144.2:p.Pro499Ser
NM_001201401.2:c.1426C>T	NP_001188330.1:p.Pro476Ser
NM_001201402.2:c.1417C>T	NP_001188331.1:p.Pro473Ser