Canonical Allele Identifier: CA349988570
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565389T>A , CM000664.2:g.189565389T>A GRCh38
NC_000002.11:g.190430115T>A , CM000664.1:g.190430115T>A GRCh37
NC_000002.10:g.190138360T>A NCBI36
NG_009027.1:g.20423A>T , LRG_837:g.20423A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.725A>T MANE Select ENSP00000261024.3:p.Glu242Val
ENST00000261024.6:c.725A>T ENSP00000261024.2:p.Glu242Val
NM_014585.5:c.725A>T , LRG_837t1:c.725A>T NP_055400.1:p.Glu242Val
XM_005246505.1:c.605A>T XP_005246562.1:p.Glu202Val
XM_005246505.2:c.605A>T XP_005246562.1:p.Glu202Val
XM_017003938.2:c.605A>T XP_016859427.1:p.Glu202Val
NM_014585.6:c.725A>T MANE Select NP_055400.1:p.Glu242Val