Canonical Allele Identifier: CA361139514
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379708T>G , CM000667.2:g.139379708T>G GRCh38
NC_000005.9:g.138715397T>G , CM000667.1:g.138715397T>G GRCh37
NC_000005.8:g.138743296T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.895A>C MANE Select ENSP00000302701.4:p.Ile299Leu
ENST00000348729.7:c.895A>C ENSP00000302701.4:p.Ile299Leu
ENST00000353963.7:c.907A>C ENSP00000302851.5:p.Ile303Leu
ENST00000504513.1:c.164+248A>C
ENST00000506512.1:n.506A>C
NM_005847.4:c.895A>C NP_005838.3:p.Ile299Leu
NM_152685.3:c.907A>C NP_689898.2:p.Ile303Leu
XM_005272148.3:c.1015A>C XP_005272205.3:p.Ile339Leu
XM_005272149.3:c.1003A>C XP_005272206.3:p.Ile335Leu
XM_006714741.2:c.1015A>C XP_006714804.2:p.Ile339Leu
XM_011543765.1:c.1015A>C XP_011542067.1:p.Ile339Leu
XM_011543766.1:c.796A>C XP_011542068.1:p.Ile266Leu
XM_011543767.1:c.700A>C XP_011542069.1:p.Ile234Leu
XM_011543768.1:c.580A>C XP_011542070.1:p.Ile194Leu
XM_011543769.1:c.190A>C XP_011542071.1:p.Ile64Leu
XM_005272149.4:c.1003A>C XP_005272206.3:p.Ile335Leu
XM_011543765.2:c.1015A>C XP_011542067.1:p.Ile339Leu
NM_005847.5:c.895A>C MANE Select NP_005838.3:p.Ile299Leu
NM_152685.4:c.907A>C NP_689898.2:p.Ile303Leu