Canonical Allele Identifier: CA2245463833

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6707297_6707299delinsCAG , CM000679.2:g.6707297_6707299delinsCAG	GRCh38
NC_000017.10:g.6610616_6610618delinsCAG , CM000679.1:g.6610616_6610618delinsCAG	GRCh37
NC_000017.9:g.6551340_6551342delinsCAG	NCBI36
NG_034220.1:g.11123_11125delinsCTG , LRG_1020:g.11123_11125delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.103-143_103-141delinsCTG MANE Select	ENSP00000406220.2:n.103-143_103-141delinsCTG
ENST00000293800.10:c.103-143_103-141delinsCTG	ENSP00000293800.6:n.103-143_103-141delinsCTG
ENST00000381074.8:c.103-521_103-519delinsCTG	ENSP00000370464.4:n.103-521_103-519delinsCTG
ENST00000433363.6:c.103-143_103-141delinsCTG	ENSP00000406220.2:n.103-143_103-141delinsCTG
ENST00000572094.1:c.103-143_103-141delinsCTG	ENSP00000461495.1:n.103-143_103-141delinsCTG
ENST00000572352.5:c.103-254_103-252delinsCTG	ENSP00000461622.1:n.103-254_103-252delinsCTG
ENST00000573648.5:c.103-143_103-141delinsCTG	ENSP00000459372.1:n.103-143_103-141delinsCTG
ENST00000575230.1:c.103-143_103-141delinsCTG	ENSP00000460903.1:n.103-143_103-141delinsCTG
ENST00000576323.1:n.141-151_141-149delinsCTG
NM_001143838.2:c.103-143_103-141delinsCTG	NP_001137310.1:n.103-143_103-141delinsCTG
NM_001284509.1:c.103-143_103-141delinsCTG	NP_001271438.1:n.103-143_103-141delinsCTG
NM_001284510.1:c.103-521_103-519delinsCTG	NP_001271439.1:n.103-521_103-519delinsCTG
NM_177550.4:c.103-143_103-141delinsCTG , LRG_1020t1:c.103-143_103-141delinsCTG	NP_808218.1:n.103-143_103-141delinsCTG
XM_006721504.2:c.103-254_103-252delinsCTG	XP_006721567.1:n.103-254_103-252delinsCTG
XM_011523795.1:c.103-143_103-141delinsCTG	XP_011522097.1:n.103-143_103-141delinsCTG
XM_011523795.3:c.103-143_103-141delinsCTG	XP_011522097.1:n.103-143_103-141delinsCTG
NM_001143838.3:c.103-143_103-141delinsCTG	NP_001137310.1:n.103-143_103-141delinsCTG
NM_001284509.2:c.103-143_103-141delinsCTG	NP_001271438.1:n.103-143_103-141delinsCTG
NM_001284510.2:c.103-521_103-519delinsCTG	NP_001271439.1:n.103-521_103-519delinsCTG
NM_177550.5:c.103-143_103-141delinsCTG MANE Select	NP_808218.1:n.103-143_103-141delinsCTG