Canonical Allele Identifier: CA1586303564

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379663_139379664delinsAG , CM000667.2:g.139379663_139379664delinsAG	GRCh38
NC_000005.9:g.138715352_138715353delinsAG , CM000667.1:g.138715352_138715353delinsAG	GRCh37
NC_000005.8:g.138743251_138743252delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.925+14_925+15delinsCT MANE Select	ENSP00000302701.4:n.925+14_925+15delinsCT
ENST00000348729.7:c.925+14_925+15delinsCT	ENSP00000302701.4:n.925+14_925+15delinsCT
ENST00000353963.7:c.937+14_937+15delinsCT	ENSP00000302851.5:n.937+14_937+15delinsCT
ENST00000504513.1:c.164+292_164+293delinsCT
ENST00000506512.1:n.536+14_536+15delinsCT
NM_005847.4:c.925+14_925+15delinsCT	NP_005838.3:n.925+14_925+15delinsCT
NM_152685.3:c.937+14_937+15delinsCT	NP_689898.2:n.937+14_937+15delinsCT
XM_005272148.3:c.1045+14_1045+15delinsCT	XP_005272205.3:n.1045+14_1045+15delinsCT
XM_005272149.3:c.1033+14_1033+15delinsCT	XP_005272206.3:n.1033+14_1033+15delinsCT
XM_006714741.2:c.1045+14_1045+15delinsCT	XP_006714804.2:n.1045+14_1045+15delinsCT
XM_011543765.1:c.1045+14_1045+15delinsCT	XP_011542067.1:n.1045+14_1045+15delinsCT
XM_011543766.1:c.826+14_826+15delinsCT	XP_011542068.1:n.826+14_826+15delinsCT
XM_011543767.1:c.730+14_730+15delinsCT	XP_011542069.1:n.730+14_730+15delinsCT
XM_011543768.1:c.610+14_610+15delinsCT	XP_011542070.1:n.610+14_610+15delinsCT
XM_011543769.1:c.220+14_220+15delinsCT	XP_011542071.1:n.220+14_220+15delinsCT
XM_005272149.4:c.1033+14_1033+15delinsCT	XP_005272206.3:n.1033+14_1033+15delinsCT
XM_011543765.2:c.1045+14_1045+15delinsCT	XP_011542067.1:n.1045+14_1045+15delinsCT
NM_005847.5:c.925+14_925+15delinsCT MANE Select	NP_005838.3:n.925+14_925+15delinsCT
NM_152685.4:c.937+14_937+15delinsCT	NP_689898.2:n.937+14_937+15delinsCT