Canonical Allele Identifier: CA1586303558

Gene: SLC23A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379658_139379659delinsGC , CM000667.2:g.139379658_139379659delinsGC	GRCh38
NC_000005.9:g.138715347_138715348delinsGC , CM000667.1:g.138715347_138715348delinsGC	GRCh37
NC_000005.8:g.138743246_138743247delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.925+19_925+20delinsGC MANE Select	ENSP00000302701.4:n.925+19_925+20delinsGC
ENST00000348729.7:c.925+19_925+20delinsGC	ENSP00000302701.4:n.925+19_925+20delinsGC
ENST00000353963.7:c.937+19_937+20delinsGC	ENSP00000302851.5:n.937+19_937+20delinsGC
ENST00000504513.1:c.164+297_164+298delinsGC
ENST00000506512.1:n.536+19_536+20delinsGC
NM_005847.4:c.925+19_925+20delinsGC	NP_005838.3:n.925+19_925+20delinsGC
NM_152685.3:c.937+19_937+20delinsGC	NP_689898.2:n.937+19_937+20delinsGC
XM_005272148.3:c.1045+19_1045+20delinsGC	XP_005272205.3:n.1045+19_1045+20delinsGC
XM_005272149.3:c.1033+19_1033+20delinsGC	XP_005272206.3:n.1033+19_1033+20delinsGC
XM_006714741.2:c.1045+19_1045+20delinsGC	XP_006714804.2:n.1045+19_1045+20delinsGC
XM_011543765.1:c.1045+19_1045+20delinsGC	XP_011542067.1:n.1045+19_1045+20delinsGC
XM_011543766.1:c.826+19_826+20delinsGC	XP_011542068.1:n.826+19_826+20delinsGC
XM_011543767.1:c.730+19_730+20delinsGC	XP_011542069.1:n.730+19_730+20delinsGC
XM_011543768.1:c.610+19_610+20delinsGC	XP_011542070.1:n.610+19_610+20delinsGC
XM_011543769.1:c.220+19_220+20delinsGC	XP_011542071.1:n.220+19_220+20delinsGC
XM_005272149.4:c.1033+19_1033+20delinsGC	XP_005272206.3:n.1033+19_1033+20delinsGC
XM_011543765.2:c.1045+19_1045+20delinsGC	XP_011542067.1:n.1045+19_1045+20delinsGC
NM_005847.5:c.925+19_925+20delinsGC MANE Select	NP_005838.3:n.925+19_925+20delinsGC
NM_152685.4:c.937+19_937+20delinsGC	NP_689898.2:n.937+19_937+20delinsGC