Canonical Allele Identifier: CA1315655793
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565433G= , CM000664.2:g.189565433G= GRCh38
NC_000002.11:g.190430159G= , CM000664.1:g.190430159G= GRCh37
NC_000002.10:g.190138404G= NCBI36
NG_009027.1:g.20379C= , LRG_837:g.20379C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.681C= MANE Select ENSP00000261024.3:p.Tyr227=
ENST00000261024.6:c.681C= ENSP00000261024.2:p.Tyr227=
NM_014585.5:c.681C= , LRG_837t1:c.681C= NP_055400.1:p.Tyr227=
XM_005246505.1:c.561C= XP_005246562.1:p.Tyr187=
XM_005246505.2:c.561C= XP_005246562.1:p.Tyr187=
XM_017003938.2:c.561C= XP_016859427.1:p.Tyr187=
NM_014585.6:c.681C= MANE Select NP_055400.1:p.Tyr227=