Canonical Allele Identifier: CA349989228
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571802C>G , CM000664.2:g.189571802C>G GRCh38
NC_000002.11:g.190436528C>G , CM000664.1:g.190436528C>G GRCh37
NC_000002.10:g.190144773C>G NCBI36
NG_009027.1:g.14010G>C , LRG_837:g.14010G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.427G>C MANE Select ENSP00000261024.3:p.Ala143Pro
ENST00000261024.6:c.427G>C ENSP00000261024.2:p.Ala143Pro
ENST00000427241.5:c.427G>C ENSP00000390005.1:p.Ala143Pro
NM_014585.5:c.427G>C , LRG_837t1:c.427G>C NP_055400.1:p.Ala143Pro
XM_005246505.1:c.307G>C XP_005246562.1:p.Ala103Pro
XM_005246505.2:c.307G>C XP_005246562.1:p.Ala103Pro
XM_017003938.2:c.307G>C XP_016859427.1:p.Ala103Pro
NM_014585.6:c.427G>C MANE Select NP_055400.1:p.Ala143Pro