Canonical Allele Identifier: CA1315653789
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575293A= , CM000664.2:g.189575293A= GRCh38
NC_000002.11:g.190440019A= , CM000664.1:g.190440019A= GRCh37
NC_000002.10:g.190148264A= NCBI36
NG_009027.1:g.10519T= , LRG_837:g.10519T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.139T= MANE Select ENSP00000261024.3:p.Ser47=
ENST00000261024.6:c.139T= ENSP00000261024.2:p.Ser47=
ENST00000418714.1:n.580T=
ENST00000427241.5:c.139T= ENSP00000390005.1:p.Ser47=
ENST00000455320.5:c.139T= ENSP00000413549.1:p.Ser47=
ENST00000479598.5:n.420T=
NM_014585.5:c.139T= , LRG_837t1:c.139T= NP_055400.1:p.Ser47=
XM_005246505.1:c.19T= XP_005246562.1:p.Ser7=
XM_005246505.2:c.19T= XP_005246562.1:p.Ser7=
XM_017003938.2:c.19T= XP_016859427.1:p.Ser7=
NM_014585.6:c.139T= MANE Select NP_055400.1:p.Ser47=