Canonical Allele Identifier: CA1586303629

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379707A= , CM000667.2:g.139379707A=	GRCh38
NC_000005.9:g.138715396A= , CM000667.1:g.138715396A=	GRCh37
NC_000005.8:g.138743295A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.896T= MANE Select	ENSP00000302701.4:p.Ile299=
ENST00000348729.7:c.896T=	ENSP00000302701.4:p.Ile299=
ENST00000353963.7:c.908T=	ENSP00000302851.5:p.Ile303=
ENST00000504513.1:c.164+249T=
ENST00000506512.1:n.507T=
NM_005847.4:c.896T=	NP_005838.3:p.Ile299=
NM_152685.3:c.908T=	NP_689898.2:p.Ile303=
XM_005272148.3:c.1016T=	XP_005272205.3:p.Ile339=
XM_005272149.3:c.1004T=	XP_005272206.3:p.Ile335=
XM_006714741.2:c.1016T=	XP_006714804.2:p.Ile339=
XM_011543765.1:c.1016T=	XP_011542067.1:p.Ile339=
XM_011543766.1:c.797T=	XP_011542068.1:p.Ile266=
XM_011543767.1:c.701T=	XP_011542069.1:p.Ile234=
XM_011543768.1:c.581T=	XP_011542070.1:p.Ile194=
XM_011543769.1:c.191T=	XP_011542071.1:p.Ile64=
XM_005272149.4:c.1004T=	XP_005272206.3:p.Ile335=
XM_011543765.2:c.1016T=	XP_011542067.1:p.Ile339=
NM_005847.5:c.896T= MANE Select	NP_005838.3:p.Ile299=
NM_152685.4:c.908T=	NP_689898.2:p.Ile303=