Canonical Allele Identifier: CA390749504

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442760A>T (hg19) ; chr14:g.87976416A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976416A>T , CM000676.2:g.87976416A>T	GRCh38
NC_000014.8:g.88442760A>T , CM000676.1:g.88442760A>T	GRCh37
NC_000014.7:g.87512513A>T	NCBI36
NG_011853.2:g.22148T>A
NG_011853.3:g.22148T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.694T>A MANE Select	ENSP00000261304.2:p.Ser232Thr
ENST00000261304.6:c.694T>A	ENSP00000261304.2:p.Ser232Thr
ENST00000393568.8:c.625T>A	ENSP00000377198.4:p.Ser209Thr
ENST00000393569.6:c.616T>A	ENSP00000377199.2:p.Ser206Thr
ENST00000474294.6:n.684T>A
ENST00000477716.3:n.449T>A
ENST00000544807.6:c.526T>A	ENSP00000437513.2:p.Ser176Thr
ENST00000554916.5:n.573T>A
ENST00000555000.5:c.61T>A	ENSP00000450472.1:p.Ser21Thr
ENST00000557316.5:c.*92T>A	ENSP00000452314.1:n.*92T>A
ENST00000622264.4:c.684T>A
NM_000153.3:c.694T>A	NP_000144.2:p.Ser232Thr
NM_001201401.1:c.625T>A	NP_001188330.1:p.Ser209Thr
NM_001201402.1:c.616T>A	NP_001188331.1:p.Ser206Thr
XM_011536618.1:c.526T>A	XP_011534920.1:p.Ser176Thr
XM_011536618.2:c.526T>A	XP_011534920.1:p.Ser176Thr
NM_000153.4:c.694T>A MANE Select	NP_000144.2:p.Ser232Thr
NM_001201401.2:c.625T>A	NP_001188330.1:p.Ser209Thr
NM_001201402.2:c.616T>A	NP_001188331.1:p.Ser206Thr