Canonical Allele Identifier: CA361139438
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379690T>G , CM000667.2:g.139379690T>G GRCh38
NC_000005.9:g.138715379T>G , CM000667.1:g.138715379T>G GRCh37
NC_000005.8:g.138743278T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.913A>C MANE Select ENSP00000302701.4:p.Ile305Leu
ENST00000348729.7:c.913A>C ENSP00000302701.4:p.Ile305Leu
ENST00000353963.7:c.925A>C ENSP00000302851.5:p.Ile309Leu
ENST00000504513.1:c.164+266A>C
ENST00000506512.1:n.524A>C
NM_005847.4:c.913A>C NP_005838.3:p.Ile305Leu
NM_152685.3:c.925A>C NP_689898.2:p.Ile309Leu
XM_005272148.3:c.1033A>C XP_005272205.3:p.Ile345Leu
XM_005272149.3:c.1021A>C XP_005272206.3:p.Ile341Leu
XM_006714741.2:c.1033A>C XP_006714804.2:p.Ile345Leu
XM_011543765.1:c.1033A>C XP_011542067.1:p.Ile345Leu
XM_011543766.1:c.814A>C XP_011542068.1:p.Ile272Leu
XM_011543767.1:c.718A>C XP_011542069.1:p.Ile240Leu
XM_011543768.1:c.598A>C XP_011542070.1:p.Ile200Leu
XM_011543769.1:c.208A>C XP_011542071.1:p.Ile70Leu
XM_005272149.4:c.1021A>C XP_005272206.3:p.Ile341Leu
XM_011543765.2:c.1033A>C XP_011542067.1:p.Ile345Leu
NM_005847.5:c.913A>C MANE Select NP_005838.3:p.Ile305Leu
NM_152685.4:c.925A>C NP_689898.2:p.Ile309Leu