Canonical Allele Identifier: CA361139435
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.913A>T MANE Select ENSP00000302701.4:p.Ile305Phe
ENST00000348729.7:c.913A>T ENSP00000302701.4:p.Ile305Phe
ENST00000353963.7:c.925A>T ENSP00000302851.5:p.Ile309Phe
ENST00000504513.1:c.164+266A>T
ENST00000506512.1:n.524A>T
NM_005847.4:c.913A>T NP_005838.3:p.Ile305Phe
NM_152685.3:c.925A>T NP_689898.2:p.Ile309Phe
XM_005272148.3:c.1033A>T XP_005272205.3:p.Ile345Phe
XM_005272149.3:c.1021A>T XP_005272206.3:p.Ile341Phe
XM_006714741.2:c.1033A>T XP_006714804.2:p.Ile345Phe
XM_011543765.1:c.1033A>T XP_011542067.1:p.Ile345Phe
XM_011543766.1:c.814A>T XP_011542068.1:p.Ile272Phe
XM_011543767.1:c.718A>T XP_011542069.1:p.Ile240Phe
XM_011543768.1:c.598A>T XP_011542070.1:p.Ile200Phe
XM_011543769.1:c.208A>T XP_011542071.1:p.Ile70Phe
XM_005272149.4:c.1021A>T XP_005272206.3:p.Ile341Phe
XM_011543765.2:c.1033A>T XP_011542067.1:p.Ile345Phe
NM_005847.5:c.913A>T MANE Select NP_005838.3:p.Ile305Phe
NM_152685.4:c.925A>T NP_689898.2:p.Ile309Phe