Canonical Allele Identifier: CA361139525
Gene: SLC23A1 HGNC NCBI

Linked Data

dbSNP Id: rs1182577323

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379710G>T , CM000667.2:g.139379710G>T GRCh38
NC_000005.9:g.138715399G>T , CM000667.1:g.138715399G>T GRCh37
NC_000005.8:g.138743298G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.893C>A MANE Select ENSP00000302701.4:p.Ala298Asp
ENST00000348729.7:c.893C>A ENSP00000302701.4:p.Ala298Asp
ENST00000353963.7:c.905C>A ENSP00000302851.5:p.Ala302Asp
ENST00000504513.1:c.164+246C>A
ENST00000506512.1:n.504C>A
NM_005847.4:c.893C>A NP_005838.3:p.Ala298Asp
NM_152685.3:c.905C>A NP_689898.2:p.Ala302Asp
XM_005272148.3:c.1013C>A XP_005272205.3:p.Ala338Asp
XM_005272149.3:c.1001C>A XP_005272206.3:p.Ala334Asp
XM_006714741.2:c.1013C>A XP_006714804.2:p.Ala338Asp
XM_011543765.1:c.1013C>A XP_011542067.1:p.Ala338Asp
XM_011543766.1:c.794C>A XP_011542068.1:p.Ala265Asp
XM_011543767.1:c.698C>A XP_011542069.1:p.Ala233Asp
XM_011543768.1:c.578C>A XP_011542070.1:p.Ala193Asp
XM_011543769.1:c.188C>A XP_011542071.1:p.Ala63Asp
XM_005272149.4:c.1001C>A XP_005272206.3:p.Ala334Asp
XM_011543765.2:c.1013C>A XP_011542067.1:p.Ala338Asp
NM_005847.5:c.893C>A MANE Select NP_005838.3:p.Ala298Asp
NM_152685.4:c.905C>A NP_689898.2:p.Ala302Asp