Canonical Allele Identifier: CA361139572
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379717T>G , CM000667.2:g.139379717T>G GRCh38
NC_000005.9:g.138715406T>G , CM000667.1:g.138715406T>G GRCh37
NC_000005.8:g.138743305T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.886A>C MANE Select ENSP00000302701.4:p.Ile296Leu
ENST00000348729.7:c.886A>C ENSP00000302701.4:p.Ile296Leu
ENST00000353963.7:c.898A>C ENSP00000302851.5:p.Ile300Leu
ENST00000504513.1:c.164+239A>C
ENST00000506512.1:n.497A>C
NM_005847.4:c.886A>C NP_005838.3:p.Ile296Leu
NM_152685.3:c.898A>C NP_689898.2:p.Ile300Leu
XM_005272148.3:c.1006A>C XP_005272205.3:p.Ile336Leu
XM_005272149.3:c.994A>C XP_005272206.3:p.Ile332Leu
XM_006714741.2:c.1006A>C XP_006714804.2:p.Ile336Leu
XM_011543765.1:c.1006A>C XP_011542067.1:p.Ile336Leu
XM_011543766.1:c.787A>C XP_011542068.1:p.Ile263Leu
XM_011543767.1:c.691A>C XP_011542069.1:p.Ile231Leu
XM_011543768.1:c.571A>C XP_011542070.1:p.Ile191Leu
XM_011543769.1:c.181A>C XP_011542071.1:p.Ile61Leu
XM_005272149.4:c.994A>C XP_005272206.3:p.Ile332Leu
XM_011543765.2:c.1006A>C XP_011542067.1:p.Ile336Leu
NM_005847.5:c.886A>C MANE Select NP_005838.3:p.Ile296Leu
NM_152685.4:c.898A>C NP_689898.2:p.Ile300Leu