Canonical Allele Identifier: CA1315654401
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564119A= , CM000664.2:g.189564119A= GRCh38
NC_000002.11:g.190428845A= , CM000664.1:g.190428845A= GRCh37
NC_000002.10:g.190137090A= NCBI36
NG_009027.1:g.21693T= , LRG_837:g.21693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.867T= MANE Select ENSP00000261024.3:p.Ala289=
ENST00000261024.6:c.867T= ENSP00000261024.2:p.Ala289=
NM_014585.5:c.867T= , LRG_837t1:c.867T= NP_055400.1:p.Ala289=
XM_005246505.1:c.747T= XP_005246562.1:p.Ala249=
XM_005246505.2:c.747T= XP_005246562.1:p.Ala249=
XM_017003938.2:c.747T= XP_016859427.1:p.Ala249=
NM_014585.6:c.867T= MANE Select NP_055400.1:p.Ala289=