Canonical Allele Identifier: CA1315653806
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563607G= , CM000664.2:g.189563607G= GRCh38
NC_000002.11:g.190428333G= , CM000664.1:g.190428333G= GRCh37
NC_000002.10:g.190136578G= NCBI36
NG_009027.1:g.22205C= , LRG_837:g.22205C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1379C= MANE Select ENSP00000261024.3:p.Ala460=
ENST00000261024.6:c.1379C= ENSP00000261024.2:p.Ala460=
NM_014585.5:c.1379C= , LRG_837t1:c.1379C= NP_055400.1:p.Ala460=
XM_005246505.1:c.1259C= XP_005246562.1:p.Ala420=
XM_005246505.2:c.1259C= XP_005246562.1:p.Ala420=
XM_017003938.2:c.1259C= XP_016859427.1:p.Ala420=
NM_014585.6:c.1379C= MANE Select NP_055400.1:p.Ala460=