Canonical Allele Identifier: CA2245463330

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6706928T= , CM000679.2:g.6706928T=	GRCh38
NC_000017.10:g.6610247T= , CM000679.1:g.6610247T=	GRCh37
NC_000017.9:g.6550971T=	NCBI36
NG_034220.1:g.11494A= , LRG_1020:g.11494A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.231+100A= MANE Select	ENSP00000406220.2:n.231+100A=
ENST00000293800.10:c.231+100A=	ENSP00000293800.6:n.231+100A=
ENST00000381074.8:c.103-150A=	ENSP00000370464.4:n.103-150A=
ENST00000433363.6:c.231+100A=	ENSP00000406220.2:n.231+100A=
ENST00000572094.1:c.227+104A=	ENSP00000461495.1:n.227+104A=
ENST00000572352.5:c.120+100A=	ENSP00000461622.1:n.120+100A=
ENST00000573648.5:c.231+100A=	ENSP00000459372.1:n.231+100A=
ENST00000575230.1:c.232-28A=	ENSP00000460903.1:n.232-28A=
ENST00000576323.1:n.261+100A=
NM_001143838.2:c.231+100A=	NP_001137310.1:n.231+100A=
NM_001284509.1:c.231+100A=	NP_001271438.1:n.231+100A=
NM_001284510.1:c.103-150A=	NP_001271439.1:n.103-150A=
NM_177550.4:c.231+100A= , LRG_1020t1:c.231+100A=	NP_808218.1:n.231+100A=
XM_006721504.2:c.120+100A=	XP_006721567.1:n.120+100A=
XM_011523795.1:c.231+100A=	XP_011522097.1:n.231+100A=
XM_011523795.3:c.231+100A=	XP_011522097.1:n.231+100A=
NM_001143838.3:c.231+100A=	NP_001137310.1:n.231+100A=
NM_001284509.2:c.231+100A=	NP_001271438.1:n.231+100A=
NM_001284510.2:c.103-150A=	NP_001271439.1:n.103-150A=
NM_177550.5:c.231+100A= MANE Select	NP_808218.1:n.231+100A=