Canonical Allele Identifier: CA390749774

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442820T>G (hg19) ; chr14:g.87976476T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976476T>G , CM000676.2:g.87976476T>G	GRCh38
NC_000014.8:g.88442820T>G , CM000676.1:g.88442820T>G	GRCh37
NC_000014.7:g.87512573T>G	NCBI36
NG_011853.2:g.22088A>C
NG_011853.3:g.22088A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.634A>C MANE Select	ENSP00000261304.2:p.Met212Leu
ENST00000261304.6:c.634A>C	ENSP00000261304.2:p.Met212Leu
ENST00000393568.8:c.565A>C	ENSP00000377198.4:p.Met189Leu
ENST00000393569.6:c.556A>C	ENSP00000377199.2:p.Met186Leu
ENST00000474294.6:n.624A>C
ENST00000477716.3:n.389A>C
ENST00000544807.6:c.466A>C	ENSP00000437513.2:p.Met156Leu
ENST00000554916.5:n.513A>C
ENST00000555000.5:c.1A>C	ENSP00000450472.1:p.Met1Leu
ENST00000557316.5:c.*32A>C	ENSP00000452314.1:n.*32A>C
ENST00000622264.4:c.624A>C
NM_000153.3:c.634A>C	NP_000144.2:p.Met212Leu
NM_001201401.1:c.565A>C	NP_001188330.1:p.Met189Leu
NM_001201402.1:c.556A>C	NP_001188331.1:p.Met186Leu
XM_011536618.1:c.466A>C	XP_011534920.1:p.Met156Leu
XM_011536618.2:c.466A>C	XP_011534920.1:p.Met156Leu
NM_000153.4:c.634A>C MANE Select	NP_000144.2:p.Met212Leu
NM_001201401.2:c.565A>C	NP_001188330.1:p.Met189Leu
NM_001201402.2:c.556A>C	NP_001188331.1:p.Met186Leu