Canonical Allele Identifier: CA1315653699
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575208A= , CM000664.2:g.189575208A= GRCh38
NC_000002.11:g.190439934A= , CM000664.1:g.190439934A= GRCh37
NC_000002.10:g.190148179A= NCBI36
NG_009027.1:g.10604T= , LRG_837:g.10604T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.224T= MANE Select ENSP00000261024.3:p.Leu75=
ENST00000261024.6:c.224T= ENSP00000261024.2:p.Leu75=
ENST00000418714.1:n.665T=
ENST00000427241.5:c.224T= ENSP00000390005.1:p.Leu75=
ENST00000479598.5:n.505T=
NM_014585.5:c.224T= , LRG_837t1:c.224T= NP_055400.1:p.Leu75=
XM_005246505.1:c.104T= XP_005246562.1:p.Leu35=
XM_005246505.2:c.104T= XP_005246562.1:p.Leu35=
XM_017003938.2:c.104T= XP_016859427.1:p.Leu35=
NM_014585.6:c.224T= MANE Select NP_055400.1:p.Leu75=