Canonical Allele Identifier: CA1586303517
Gene: SLC23A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379627_139379644delinsCTCATAGGTGGTCTCAGT , CM000667.2:g.139379627_139379644delinsCTCATAGGTGGTCTCAGT GRCh38
NC_000005.9:g.138715316_138715333delinsCTCATAGGTGGTCTCAGT , CM000667.1:g.138715316_138715333delinsCTCATAGGTGGTCTCAGT GRCh37
NC_000005.8:g.138743215_138743232delinsCTCATAGGTGGTCTCAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.925+34_925+51delinsACTGAGACCACCTATGAG MANE Select ENSP00000302701.4:n.925+34_925+51delinsACTGAGACCACCTATGAG
ENST00000348729.7:c.925+34_925+51delinsACTGAGACCACCTATGAG ENSP00000302701.4:n.925+34_925+51delinsACTGAGACCACCTATGAG
ENST00000353963.7:c.937+34_937+51delinsACTGAGACCACCTATGAG ENSP00000302851.5:n.937+34_937+51delinsACTGAGACCACCTATGAG
ENST00000504513.1:c.165-290_165-273delinsACTGAGACCACCTATGAG
ENST00000506512.1:n.536+34_536+51delinsACTGAGACCACCTATGAG
NM_005847.4:c.925+34_925+51delinsACTGAGACCACCTATGAG NP_005838.3:n.925+34_925+51delinsACTGAGACCACCTATGAG
NM_152685.3:c.937+34_937+51delinsACTGAGACCACCTATGAG NP_689898.2:n.937+34_937+51delinsACTGAGACCACCTATGAG
XM_005272148.3:c.1045+34_1045+51delinsACTGAGACCACCTATGAG XP_005272205.3:n.1045+34_1045+51delinsACTGAGACCACCTATGAG
XM_005272149.3:c.1033+34_1033+51delinsACTGAGACCACCTATGAG XP_005272206.3:n.1033+34_1033+51delinsACTGAGACCACCTATGAG
XM_006714741.2:c.1045+34_1045+51delinsACTGAGACCACCTATGAG XP_006714804.2:n.1045+34_1045+51delinsACTGAGACCACCTATGAG
XM_011543765.1:c.1045+34_1045+51delinsACTGAGACCACCTATGAG XP_011542067.1:n.1045+34_1045+51delinsACTGAGACCACCTATGAG
XM_011543766.1:c.826+34_826+51delinsACTGAGACCACCTATGAG XP_011542068.1:n.826+34_826+51delinsACTGAGACCACCTATGAG
XM_011543767.1:c.730+34_730+51delinsACTGAGACCACCTATGAG XP_011542069.1:n.730+34_730+51delinsACTGAGACCACCTATGAG
XM_011543768.1:c.610+34_610+51delinsACTGAGACCACCTATGAG XP_011542070.1:n.610+34_610+51delinsACTGAGACCACCTATGAG
XM_011543769.1:c.220+34_220+51delinsACTGAGACCACCTATGAG XP_011542071.1:n.220+34_220+51delinsACTGAGACCACCTATGAG
XM_005272149.4:c.1033+34_1033+51delinsACTGAGACCACCTATGAG XP_005272206.3:n.1033+34_1033+51delinsACTGAGACCACCTATGAG
XM_011543765.2:c.1045+34_1045+51delinsACTGAGACCACCTATGAG XP_011542067.1:n.1045+34_1045+51delinsACTGAGACCACCTATGAG
NM_005847.5:c.925+34_925+51delinsACTGAGACCACCTATGAG MANE Select NP_005838.3:n.925+34_925+51delinsACTGAGACCACCTATGAG
NM_152685.4:c.937+34_937+51delinsACTGAGACCACCTATGAG NP_689898.2:n.937+34_937+51delinsACTGAGACCACCTATGAG