Canonical Allele Identifier: CA1315655789
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565425G= , CM000664.2:g.189565425G= GRCh38
NC_000002.11:g.190430151G= , CM000664.1:g.190430151G= GRCh37
NC_000002.10:g.190138396G= NCBI36
NG_009027.1:g.20387C= , LRG_837:g.20387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.689C= MANE Select ENSP00000261024.3:p.Thr230=
ENST00000261024.6:c.689C= ENSP00000261024.2:p.Thr230=
NM_014585.5:c.689C= , LRG_837t1:c.689C= NP_055400.1:p.Thr230=
XM_005246505.1:c.569C= XP_005246562.1:p.Thr190=
XM_005246505.2:c.569C= XP_005246562.1:p.Thr190=
XM_017003938.2:c.569C= XP_016859427.1:p.Thr190=
NM_014585.6:c.689C= MANE Select NP_055400.1:p.Thr230=