Canonical Allele Identifier: CA430367378
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190436526T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571800T>A , CM000664.2:g.189571800T>A GRCh38
NC_000002.11:g.190436526T>A , CM000664.1:g.190436526T>A GRCh37
NC_000002.10:g.190144771T>A NCBI36
NG_009027.1:g.14012A>T , LRG_837:g.14012A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.429A>T MANE Select ENSP00000261024.3:p.Ala143=
ENST00000261024.6:c.429A>T ENSP00000261024.2:p.Ala143=
ENST00000427241.5:c.429A>T ENSP00000390005.1:p.Ala143=
NM_014585.5:c.429A>T , LRG_837t1:c.429A>T NP_055400.1:p.Ala143=
XM_005246505.1:c.309A>T XP_005246562.1:p.Ala103=
XM_005246505.2:c.309A>T XP_005246562.1:p.Ala103=
XM_017003938.2:c.309A>T XP_016859427.1:p.Ala103=
NM_014585.6:c.429A>T MANE Select NP_055400.1:p.Ala143=