Canonical Allele Identifier: CA1315654057
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563802C= , CM000664.2:g.189563802C= GRCh38
NC_000002.11:g.190428528C= , CM000664.1:g.190428528C= GRCh37
NC_000002.10:g.190136773C= NCBI36
NG_009027.1:g.22010G= , LRG_837:g.22010G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1184G= MANE Select ENSP00000261024.3:p.Gly395=
ENST00000261024.6:c.1184G= ENSP00000261024.2:p.Gly395=
NM_014585.5:c.1184G= , LRG_837t1:c.1184G= NP_055400.1:p.Gly395=
XM_005246505.1:c.1064G= XP_005246562.1:p.Gly355=
XM_005246505.2:c.1064G= XP_005246562.1:p.Gly355=
XM_017003938.2:c.1064G= XP_016859427.1:p.Gly355=
NM_014585.6:c.1184G= MANE Select NP_055400.1:p.Gly395=