Canonical Allele Identifier: CA9891527

Gene: SLC13A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46596148C>T , CM000682.2:g.46596148C>T	GRCh38
NC_000020.10:g.45224787C>T , CM000682.1:g.45224787C>T	GRCh37
NC_000020.9:g.44658194C>T	NCBI36
NG_047182.1:g.93338G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022829.6:c.794+9G>A MANE Select	NP_073740.2:n.794+9G>A
ENST00000279027.9:c.794+9G>A MANE Select	ENSP00000279027.4:n.794+9G>A
NM_001011554.2:c.653+9G>A	NP_001011554.1:n.653+9G>A
NM_001011554.3:c.653+9G>A	NP_001011554.1:n.653+9G>A
NM_001193339.1:c.727+9G>A	NP_001180268.1:n.727+9G>A
NM_001193339.2:c.727+9G>A	NP_001180268.1:n.727+9G>A
NM_001193340.1:c.653+9G>A	NP_001180269.1:n.653+9G>A
NM_001193340.2:c.653+9G>A	NP_001180269.1:n.653+9G>A
NM_001193342.1:c.500+9G>A	NP_001180271.1:n.500+9G>A
NM_001193342.2:c.500+9G>A	NP_001180271.1:n.500+9G>A
NM_022829.5:c.794+9G>A	NP_073740.2:n.794+9G>A
ENST00000279027.8:c.794+9G>A	ENSP00000279027.4:n.794+9G>A
ENST00000290317.9:c.653+9G>A	ENSP00000290317.5:n.653+9G>A
ENST00000372121.5:c.586+9G>A	ENSP00000361193.2:n.586+9G>A
ENST00000413164.6:c.727+9G>A	ENSP00000415852.2:n.727+9G>A
ENST00000420568.5:c.616+9G>A	ENSP00000395095.1:n.616+9G>A
ENST00000450298.5:c.282+9G>A
ENST00000468915.5:c.653+9G>A	ENSP00000417784.1:n.653+9G>A
ENST00000472148.5:c.653+9G>A	ENSP00000420177.1:n.653+9G>A
ENST00000495082.5:c.653+9G>A	ENSP00000419621.1:n.653+9G>A