Canonical Allele Identifier: CA361139576
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379718G>T , CM000667.2:g.139379718G>T GRCh38
NC_000005.9:g.138715407G>T , CM000667.1:g.138715407G>T GRCh37
NC_000005.8:g.138743306G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.885C>A MANE Select ENSP00000302701.4:p.Asp295Glu
ENST00000348729.7:c.885C>A ENSP00000302701.4:p.Asp295Glu
ENST00000353963.7:c.897C>A ENSP00000302851.5:p.Asp299Glu
ENST00000504513.1:c.164+238C>A
ENST00000506512.1:n.496C>A
NM_005847.4:c.885C>A NP_005838.3:p.Asp295Glu
NM_152685.3:c.897C>A NP_689898.2:p.Asp299Glu
XM_005272148.3:c.1005C>A XP_005272205.3:p.Asp335Glu
XM_005272149.3:c.993C>A XP_005272206.3:p.Asp331Glu
XM_006714741.2:c.1005C>A XP_006714804.2:p.Asp335Glu
XM_011543765.1:c.1005C>A XP_011542067.1:p.Asp335Glu
XM_011543766.1:c.786C>A XP_011542068.1:p.Asp262Glu
XM_011543767.1:c.690C>A XP_011542069.1:p.Asp230Glu
XM_011543768.1:c.570C>A XP_011542070.1:p.Asp190Glu
XM_011543769.1:c.180C>A XP_011542071.1:p.Asp60Glu
XM_005272149.4:c.993C>A XP_005272206.3:p.Asp331Glu
XM_011543765.2:c.1005C>A XP_011542067.1:p.Asp335Glu
NM_005847.5:c.885C>A MANE Select NP_005838.3:p.Asp295Glu
NM_152685.4:c.897C>A NP_689898.2:p.Asp299Glu