Canonical Allele Identifier: CA1586303637

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379712C= , CM000667.2:g.139379712C=	GRCh38
NC_000005.9:g.138715401C= , CM000667.1:g.138715401C=	GRCh37
NC_000005.8:g.138743300C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.891G= MANE Select	ENSP00000302701.4:p.Met297=
ENST00000348729.7:c.891G=	ENSP00000302701.4:p.Met297=
ENST00000353963.7:c.903G=	ENSP00000302851.5:p.Met301=
ENST00000504513.1:c.164+244G=
ENST00000506512.1:n.502G=
NM_005847.4:c.891G=	NP_005838.3:p.Met297=
NM_152685.3:c.903G=	NP_689898.2:p.Met301=
XM_005272148.3:c.1011G=	XP_005272205.3:p.Met337=
XM_005272149.3:c.999G=	XP_005272206.3:p.Met333=
XM_006714741.2:c.1011G=	XP_006714804.2:p.Met337=
XM_011543765.1:c.1011G=	XP_011542067.1:p.Met337=
XM_011543766.1:c.792G=	XP_011542068.1:p.Met264=
XM_011543767.1:c.696G=	XP_011542069.1:p.Met232=
XM_011543768.1:c.576G=	XP_011542070.1:p.Met192=
XM_011543769.1:c.186G=	XP_011542071.1:p.Met62=
XM_005272149.4:c.999G=	XP_005272206.3:p.Met333=
XM_011543765.2:c.1011G=	XP_011542067.1:p.Met337=
NM_005847.5:c.891G= MANE Select	NP_005838.3:p.Met297=
NM_152685.4:c.903G=	NP_689898.2:p.Met301=