Canonical Allele Identifier: CA11098198
Gene: SLC11A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1059823

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218395121A>G , CM000664.2:g.218395121A>G GRCh38
NC_000002.11:g.219259844A>G , CM000664.1:g.219259844A>G GRCh37
NC_000002.10:g.218968088A>G NCBI36
NG_012128.1:g.18093A>G
NG_030418.1:g.1784A>G

Transcript Alleles

HGVS Amino-acid change
NM_000578.3:c.*86A>G VV NP_000569.3:p.=
XM_005246793.2:c.*86A>G XP_005246850.1:p.=
XM_005246794.2:c.*86A>G XP_005246851.1:p.=
XM_006712709.2:c.*86A>G XP_006712772.1:p.=
XM_006712710.2:c.*86A>G XP_006712773.1:p.=
XM_006712711.2:c.*86A>G XP_006712774.1:p.=
XM_011511684.1:c.*86A>G XP_011509986.1:p.=
XM_011511685.1:c.*86A>G XP_011509987.1:p.=
XM_005246793.4:c.*86A>G
XM_005246794.4:c.*86A>G
XM_006712709.4:c.*86A>G
XM_006712710.4:c.*86A>G
XM_006712711.4:c.*86A>G
XM_011511684.3:c.*86A>G
XM_011511685.3:c.*86A>G
XM_017004765.2:c.*86A>G XP_016860254.1:p.=
XM_017004766.2:c.*86A>G XP_016860255.1:p.=
XM_017004767.2:c.*86A>G XP_016860256.1:p.=
XR_427107.3:n.2754A>G
XR_427108.4:n.3065A>G
ENST00000233202.10:c.*86A>G ENSP00000233202.6:p.=
ENST00000354352.9:c.*1321A>G ENSP00000346320.5:p.=
ENST00000465984.5:n.2160+55A>G
ENST00000468221.5:n.4866A>G