Canonical Allele Identifier: CA1315653744
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575243G= , CM000664.2:g.189575243G= GRCh38
NC_000002.11:g.190439969G= , CM000664.1:g.190439969G= GRCh37
NC_000002.10:g.190148214G= NCBI36
NG_009027.1:g.10569C= , LRG_837:g.10569C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.189C= MANE Select ENSP00000261024.3:p.Val63=
ENST00000261024.6:c.189C= ENSP00000261024.2:p.Val63=
ENST00000418714.1:n.630C=
ENST00000427241.5:c.189C= ENSP00000390005.1:p.Val63=
ENST00000479598.5:n.470C=
NM_014585.5:c.189C= , LRG_837t1:c.189C= NP_055400.1:p.Val63=
XM_005246505.1:c.69C= XP_005246562.1:p.Val23=
XM_005246505.2:c.69C= XP_005246562.1:p.Val23=
XM_017003938.2:c.69C= XP_016859427.1:p.Val23=
NM_014585.6:c.189C= MANE Select NP_055400.1:p.Val63=