Canonical Allele Identifier: CA350550932
Gene: SLC11A1 HGNC NCBI

Linked Data

dbSNP Id: rs1696683846

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218395033T>C , CM000664.2:g.218395033T>C GRCh38
NC_000002.11:g.219259756T>C , CM000664.1:g.219259756T>C GRCh37
NC_000002.10:g.218968000T>C NCBI36
NG_012128.1:g.18005T>C
NG_030418.1:g.1696T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233202.11:c.1651T>C MANE Select ENSP00000233202.6:p.Ter551Gln
ENST00000233202.10:c.1651T>C ENSP00000233202.6:p.Ter551Gln
ENST00000354352.9:c.*1233T>C ENSP00000346320.5:n.*1233T>C
ENST00000465984.5:n.2127T>C
ENST00000468221.5:n.4778T>C
NM_000578.3:c.1651T>C NP_000569.3:p.Ter551Gln
XM_005246793.2:c.1450T>C XP_005246850.1:p.Ter484Gln
XM_005246794.2:c.1297T>C XP_005246851.1:p.Ter433Gln
XM_006712709.2:c.1297T>C XP_006712772.1:p.Ter433Gln
XM_006712710.2:c.1297T>C XP_006712773.1:p.Ter433Gln
XM_006712711.2:c.1204T>C XP_006712774.1:p.Ter402Gln
XM_011511684.1:c.1324T>C XP_011509986.1:p.Ter442Gln
XM_011511685.1:c.1324T>C XP_011509987.1:p.Ter442Gln
XM_005246793.4:c.1450T>C XP_005246850.1:p.Ter484Gln
XM_005246794.4:c.1297T>C XP_005246851.1:p.Ter433Gln
XM_006712709.4:c.1297T>C XP_006712772.1:p.Ter433Gln
XM_006712710.4:c.1297T>C XP_006712773.1:p.Ter433Gln
XM_006712711.4:c.1204T>C XP_006712774.1:p.Ter402Gln
XM_011511684.3:c.1324T>C XP_011509986.1:p.Ter442Gln
XM_011511685.3:c.1324T>C XP_011509987.1:p.Ter442Gln
XM_017004765.2:c.1528T>C XP_016860254.1:p.Ter510Gln
XM_017004766.2:c.1450T>C XP_016860255.1:p.Ter484Gln
XM_017004767.2:c.1282T>C XP_016860256.1:p.Ter428Gln
XR_427107.3:n.2666T>C
XR_427108.4:n.2977T>C
NM_000578.4:c.1651T>C MANE Select NP_000569.3:p.Ter551Gln