Canonical Allele Identifier: CA390745872

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88407876A>G (hg19) ; chr14:g.87941532A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87941532A>G , CM000676.2:g.87941532A>G	GRCh38
NC_000014.8:g.88407876A>G , CM000676.1:g.88407876A>G	GRCh37
NC_000014.7:g.87477629A>G	NCBI36
NG_011853.2:g.57032T>C
NG_011853.3:g.57032T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1697T>C MANE Select	ENSP00000261304.2:p.Val566Ala
ENST00000261304.6:c.1697T>C	ENSP00000261304.2:p.Val566Ala
ENST00000393568.8:c.1628T>C	ENSP00000377198.4:p.Val543Ala
ENST00000393569.6:c.1619T>C	ENSP00000377199.2:p.Val540Ala
ENST00000544807.6:c.1529T>C	ENSP00000437513.2:p.Val510Ala
ENST00000555000.5:c.1064T>C	ENSP00000450472.1:p.Val355Ala
ENST00000555179.1:c.233T>C
ENST00000557316.5:c.*1095T>C	ENSP00000452314.1:n.*1095T>C
NM_000153.3:c.1697T>C	NP_000144.2:p.Val566Ala
NM_001201401.1:c.1628T>C	NP_001188330.1:p.Val543Ala
NM_001201402.1:c.1619T>C	NP_001188331.1:p.Val540Ala
XM_011536618.1:c.1529T>C	XP_011534920.1:p.Val510Ala
XM_011536618.2:c.1529T>C	XP_011534920.1:p.Val510Ala
NM_000153.4:c.1697T>C MANE Select	NP_000144.2:p.Val566Ala
NM_001201401.2:c.1628T>C	NP_001188330.1:p.Val543Ala
NM_001201402.2:c.1619T>C	NP_001188331.1:p.Val540Ala