Canonical Allele Identifier: CA1315653605
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575170T= , CM000664.2:g.189575170T= GRCh38
NC_000002.11:g.190439896T= , CM000664.1:g.190439896T= GRCh37
NC_000002.10:g.190148141T= NCBI36
NG_009027.1:g.10642A= , LRG_837:g.10642A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.262A= MANE Select ENSP00000261024.3:p.Arg88=
ENST00000261024.6:c.262A= ENSP00000261024.2:p.Arg88=
ENST00000418714.1:n.703A=
ENST00000427241.5:c.262A= ENSP00000390005.1:p.Arg88=
ENST00000479598.5:n.543A=
NM_014585.5:c.262A= , LRG_837t1:c.262A= NP_055400.1:p.Arg88=
XM_005246505.1:c.142A= XP_005246562.1:p.Arg48=
XM_005246505.2:c.142A= XP_005246562.1:p.Arg48=
XM_017003938.2:c.142A= XP_016859427.1:p.Arg48=
NM_014585.6:c.262A= MANE Select NP_055400.1:p.Arg88=