Canonical Allele Identifier: CA1315655765
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565414C= , CM000664.2:g.189565414C= GRCh38
NC_000002.11:g.190430140C= , CM000664.1:g.190430140C= GRCh37
NC_000002.10:g.190138385C= NCBI36
NG_009027.1:g.20398G= , LRG_837:g.20398G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.700G= MANE Select ENSP00000261024.3:p.Ala234=
ENST00000261024.6:c.700G= ENSP00000261024.2:p.Ala234=
NM_014585.5:c.700G= , LRG_837t1:c.700G= NP_055400.1:p.Ala234=
XM_005246505.1:c.580G= XP_005246562.1:p.Ala194=
XM_005246505.2:c.580G= XP_005246562.1:p.Ala194=
XM_017003938.2:c.580G= XP_016859427.1:p.Ala194=
NM_014585.6:c.700G= MANE Select NP_055400.1:p.Ala234=