Canonical Allele Identifier: CA2024278
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs776750415

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575173C>T , CM000664.2:g.189575173C>T GRCh38
NC_000002.11:g.190439899C>T , CM000664.1:g.190439899C>T GRCh37
NC_000002.10:g.190148144C>T NCBI36
NG_009027.1:g.10639G>A , LRG_837:g.10639G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.259G>A MANE Select ENSP00000261024.3:p.Ala87Thr
ENST00000261024.6:c.259G>A ENSP00000261024.2:p.Ala87Thr
ENST00000418714.1:n.700G>A
ENST00000427241.5:c.259G>A ENSP00000390005.1:p.Ala87Thr
ENST00000479598.5:n.540G>A
NM_014585.5:c.259G>A , LRG_837t1:c.259G>A NP_055400.1:p.Ala87Thr
XM_005246505.1:c.139G>A XP_005246562.1:p.Ala47Thr
XM_005246505.2:c.139G>A XP_005246562.1:p.Ala47Thr
XM_017003938.2:c.139G>A XP_016859427.1:p.Ala47Thr
NM_014585.6:c.259G>A MANE Select NP_055400.1:p.Ala87Thr