Canonical Allele Identifier: CA1315654198
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563937G= , CM000664.2:g.189563937G= GRCh38
NC_000002.11:g.190428663G= , CM000664.1:g.190428663G= GRCh37
NC_000002.10:g.190136908G= NCBI36
NG_009027.1:g.21875C= , LRG_837:g.21875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1049C= MANE Select ENSP00000261024.3:p.Ala350=
ENST00000261024.6:c.1049C= ENSP00000261024.2:p.Ala350=
NM_014585.5:c.1049C= , LRG_837t1:c.1049C= NP_055400.1:p.Ala350=
XM_005246505.1:c.929C= XP_005246562.1:p.Ala310=
XM_005246505.2:c.929C= XP_005246562.1:p.Ala310=
XM_017003938.2:c.929C= XP_016859427.1:p.Ala310=
NM_014585.6:c.1049C= MANE Select NP_055400.1:p.Ala350=