Canonical Allele Identifier: CA1586303854
Gene: SLC23A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379849T= , CM000667.2:g.139379849T= GRCh38
NC_000005.9:g.138715538T= , CM000667.1:g.138715538T= GRCh37
NC_000005.8:g.138743437T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.769-15A= MANE Select ENSP00000302701.4:n.769-15A=
ENST00000348729.7:c.769-15A= ENSP00000302701.4:n.769-15A=
ENST00000353963.7:c.781-15A= ENSP00000302851.5:n.781-15A=
ENST00000504513.1:c.164+107A=
ENST00000506512.1:n.365A=
NM_005847.4:c.769-15A= NP_005838.3:n.769-15A=
NM_152685.3:c.781-15A= NP_689898.2:n.781-15A=
XM_005272148.3:c.889-15A= XP_005272205.3:n.889-15A=
XM_005272149.3:c.877-15A= XP_005272206.3:n.877-15A=
XM_006714741.2:c.889-15A= XP_006714804.2:n.889-15A=
XM_011543765.1:c.889-15A= XP_011542067.1:n.889-15A=
XM_011543766.1:c.670-15A= XP_011542068.1:n.670-15A=
XM_011543767.1:c.574-15A= XP_011542069.1:n.574-15A=
XM_011543768.1:c.454-15A= XP_011542070.1:n.454-15A=
XM_011543769.1:c.64-15A= XP_011542071.1:n.64-15A=
XM_005272149.4:c.877-15A= XP_005272206.3:n.877-15A=
XM_011543765.2:c.889-15A= XP_011542067.1:n.889-15A=
NM_005847.5:c.769-15A= MANE Select NP_005838.3:n.769-15A=
NM_152685.4:c.781-15A= NP_689898.2:n.781-15A=