Canonical Allele Identifier: CA1315653843
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575365C= , CM000664.2:g.189575365C= GRCh38
NC_000002.11:g.190440091C= , CM000664.1:g.190440091C= GRCh37
NC_000002.10:g.190148336C= NCBI36
NG_009027.1:g.10447G= , LRG_837:g.10447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.112-45G= MANE Select ENSP00000261024.3:n.112-45G=
ENST00000261024.6:c.112-45G= ENSP00000261024.2:n.112-45G=
ENST00000418714.1:n.553-45G=
ENST00000427241.5:c.112-45G= ENSP00000390005.1:n.112-45G=
ENST00000455320.5:c.112-45G= ENSP00000413549.1:n.112-45G=
ENST00000479598.5:n.393-45G=
NM_014585.5:c.112-45G= , LRG_837t1:c.112-45G= NP_055400.1:n.112-45G=
XM_005246505.1:c.-9-45G= XP_005246562.1:n.-9-45G=
XM_005246505.2:c.-9-45G= XP_005246562.1:n.-9-45G=
XM_017003938.2:c.-9-45G= XP_016859427.1:n.-9-45G=
NM_014585.6:c.112-45G= MANE Select NP_055400.1:n.112-45G=