Canonical Allele Identifier: CA361139545
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379713A>T , CM000667.2:g.139379713A>T GRCh38
NC_000005.9:g.138715402A>T , CM000667.1:g.138715402A>T GRCh37
NC_000005.8:g.138743301A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.890T>A MANE Select ENSP00000302701.4:p.Met297Lys
ENST00000348729.7:c.890T>A ENSP00000302701.4:p.Met297Lys
ENST00000353963.7:c.902T>A ENSP00000302851.5:p.Met301Lys
ENST00000504513.1:c.164+243T>A
ENST00000506512.1:n.501T>A
NM_005847.4:c.890T>A NP_005838.3:p.Met297Lys
NM_152685.3:c.902T>A NP_689898.2:p.Met301Lys
XM_005272148.3:c.1010T>A XP_005272205.3:p.Met337Lys
XM_005272149.3:c.998T>A XP_005272206.3:p.Met333Lys
XM_006714741.2:c.1010T>A XP_006714804.2:p.Met337Lys
XM_011543765.1:c.1010T>A XP_011542067.1:p.Met337Lys
XM_011543766.1:c.791T>A XP_011542068.1:p.Met264Lys
XM_011543767.1:c.695T>A XP_011542069.1:p.Met232Lys
XM_011543768.1:c.575T>A XP_011542070.1:p.Met192Lys
XM_011543769.1:c.185T>A XP_011542071.1:p.Met62Lys
XM_005272149.4:c.998T>A XP_005272206.3:p.Met333Lys
XM_011543765.2:c.1010T>A XP_011542067.1:p.Met337Lys
NM_005847.5:c.890T>A MANE Select NP_005838.3:p.Met297Lys
NM_152685.4:c.902T>A NP_689898.2:p.Met301Lys