Canonical Allele Identifier: CA1586303657

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379720C= , CM000667.2:g.139379720C=	GRCh38
NC_000005.9:g.138715409C= , CM000667.1:g.138715409C=	GRCh37
NC_000005.8:g.138743308C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.883G= MANE Select	ENSP00000302701.4:p.Asp295=
ENST00000348729.7:c.883G=	ENSP00000302701.4:p.Asp295=
ENST00000353963.7:c.895G=	ENSP00000302851.5:p.Asp299=
ENST00000504513.1:c.164+236G=
ENST00000506512.1:n.494G=
NM_005847.4:c.883G=	NP_005838.3:p.Asp295=
NM_152685.3:c.895G=	NP_689898.2:p.Asp299=
XM_005272148.3:c.1003G=	XP_005272205.3:p.Asp335=
XM_005272149.3:c.991G=	XP_005272206.3:p.Asp331=
XM_006714741.2:c.1003G=	XP_006714804.2:p.Asp335=
XM_011543765.1:c.1003G=	XP_011542067.1:p.Asp335=
XM_011543766.1:c.784G=	XP_011542068.1:p.Asp262=
XM_011543767.1:c.688G=	XP_011542069.1:p.Asp230=
XM_011543768.1:c.568G=	XP_011542070.1:p.Asp190=
XM_011543769.1:c.178G=	XP_011542071.1:p.Asp60=
XM_005272149.4:c.991G=	XP_005272206.3:p.Asp331=
XM_011543765.2:c.1003G=	XP_011542067.1:p.Asp335=
NM_005847.5:c.883G= MANE Select	NP_005838.3:p.Asp295=
NM_152685.4:c.895G=	NP_689898.2:p.Asp299=