Canonical Allele Identifier: CA1586303587

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379683T= , CM000667.2:g.139379683T=	GRCh38
NC_000005.9:g.138715372T= , CM000667.1:g.138715372T=	GRCh37
NC_000005.8:g.138743271T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.920A= MANE Select	ENSP00000302701.4:p.Tyr307=
ENST00000348729.7:c.920A=	ENSP00000302701.4:p.Tyr307=
ENST00000353963.7:c.932A=	ENSP00000302851.5:p.Tyr311=
ENST00000504513.1:c.164+273A=
ENST00000506512.1:n.531A=
NM_005847.4:c.920A=	NP_005838.3:p.Tyr307=
NM_152685.3:c.932A=	NP_689898.2:p.Tyr311=
XM_005272148.3:c.1040A=	XP_005272205.3:p.Tyr347=
XM_005272149.3:c.1028A=	XP_005272206.3:p.Tyr343=
XM_006714741.2:c.1040A=	XP_006714804.2:p.Tyr347=
XM_011543765.1:c.1040A=	XP_011542067.1:p.Tyr347=
XM_011543766.1:c.821A=	XP_011542068.1:p.Tyr274=
XM_011543767.1:c.725A=	XP_011542069.1:p.Tyr242=
XM_011543768.1:c.605A=	XP_011542070.1:p.Tyr202=
XM_011543769.1:c.215A=	XP_011542071.1:p.Tyr72=
XM_005272149.4:c.1028A=	XP_005272206.3:p.Tyr343=
XM_011543765.2:c.1040A=	XP_011542067.1:p.Tyr347=
NM_005847.5:c.920A= MANE Select	NP_005838.3:p.Tyr307=
NM_152685.4:c.932A=	NP_689898.2:p.Tyr311=