Canonical Allele Identifier: CA1586303800

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379818A= , CM000667.2:g.139379818A=	GRCh38
NC_000005.9:g.138715507A= , CM000667.1:g.138715507A=	GRCh37
NC_000005.8:g.138743406A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000348729.8:c.785T= MANE Select	ENSP00000302701.4:p.Met262=
ENST00000348729.7:c.785T=	ENSP00000302701.4:p.Met262=
ENST00000353963.7:c.797T=	ENSP00000302851.5:p.Met266=
ENST00000504513.1:c.164+138T=
ENST00000506512.1:n.396T=
NM_005847.4:c.785T=	NP_005838.3:p.Met262=
NM_152685.3:c.797T=	NP_689898.2:p.Met266=
XM_005272148.3:c.905T=	XP_005272205.3:p.Met302=
XM_005272149.3:c.893T=	XP_005272206.3:p.Met298=
XM_006714741.2:c.905T=	XP_006714804.2:p.Met302=
XM_011543765.1:c.905T=	XP_011542067.1:p.Met302=
XM_011543766.1:c.686T=	XP_011542068.1:p.Met229=
XM_011543767.1:c.590T=	XP_011542069.1:p.Met197=
XM_011543768.1:c.470T=	XP_011542070.1:p.Met157=
XM_011543769.1:c.80T=	XP_011542071.1:p.Met27=
XM_005272149.4:c.893T=	XP_005272206.3:p.Met298=
XM_011543765.2:c.905T=	XP_011542067.1:p.Met302=
NM_005847.5:c.785T= MANE Select	NP_005838.3:p.Met262=
NM_152685.4:c.797T=	NP_689898.2:p.Met266=