Canonical Allele Identifier: CA357750006
Gene: SLC39A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102267971T>G , CM000666.2:g.102267971T>G GRCh38
NC_000004.11:g.103189128T>G , CM000666.1:g.103189128T>G GRCh37
NC_000004.10:g.103408151T>G NCBI36
NG_047177.1:g.82528A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000424970.7:c.974A>C ENSP00000394548.3:p.His325Pro
ENST00000682227.1:c.949A>C ENSP00000508363.1:p.Ile317Leu
ENST00000682243.1:c.*1095A>C ENSP00000507952.1:n.*1095A>C
ENST00000682549.1:c.974A>C ENSP00000507483.1:p.His325Pro
ENST00000682932.1:c.949A>C ENSP00000507414.1:p.Ile317Leu
ENST00000683173.1:c.*1070A>C ENSP00000508032.1:n.*1070A>C
ENST00000683221.1:c.949A>C ENSP00000508093.1:p.Ile317Leu
ENST00000683401.1:n.882A>C
ENST00000683412.1:c.949A>C ENSP00000507538.1:p.Ile317Leu
ENST00000683462.1:c.974A>C ENSP00000507170.1:p.His325Pro
ENST00000683634.1:c.*1070A>C ENSP00000507087.1:n.*1070A>C
ENST00000683706.1:c.353A>C ENSP00000506745.1:p.His118Pro
ENST00000683916.1:c.974A>C ENSP00000508106.1:p.His325Pro
ENST00000684289.1:c.*624A>C ENSP00000506748.1:n.*624A>C
ENST00000684386.1:c.*163A>C ENSP00000507611.1:n.*163A>C
ENST00000356736.5:c.949A>C MANE Select ENSP00000349174.4:p.Ile317Leu
ENST00000356736.4:c.949A>C ENSP00000349174.4:p.Ile317Leu
ENST00000394833.6:c.949A>C ENSP00000378310.2:p.Ile317Leu
ENST00000424970.6:c.949A>C ENSP00000394548.2:p.Ile317Leu
NM_001135146.1:c.949A>C NP_001128618.1:p.Ile317Leu
NM_001135147.1:c.949A>C NP_001128619.1:p.Ile317Leu
NM_001135148.1:c.748A>C NP_001128620.1:p.Ile250Leu
NM_022154.5:c.949A>C NP_071437.3:p.Ile317Leu
XM_005263177.1:c.949A>C XP_005263234.1:p.Ile317Leu
XM_011532182.1:c.307A>C XP_011530484.1:p.Ile103Leu
XM_005263177.2:c.949A>C XP_005263234.1:p.Ile317Leu
XM_017008541.1:c.748A>C XP_016864030.1:p.Ile250Leu
XM_024454184.1:c.949A>C XP_024309952.1:p.Ile317Leu
NM_001135146.2:c.949A>C MANE Select NP_001128618.1:p.Ile317Leu
NM_001135148.2:c.748A>C NP_001128620.1:p.Ile250Leu