Canonical Allele Identifier: CA357750165
Gene: SLC39A8 HGNC NCBI

Linked Data

dbSNP Id: rs1732185331

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102268043T>C , CM000666.2:g.102268043T>C GRCh38
NC_000004.11:g.103189200T>C , CM000666.1:g.103189200T>C GRCh37
NC_000004.10:g.103408223T>C NCBI36
NG_047177.1:g.82456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000424970.7:c.902A>G ENSP00000394548.3:p.Glu301Gly
ENST00000682227.1:c.877A>G ENSP00000508363.1:p.Lys293Glu
ENST00000682243.1:c.*1023A>G ENSP00000507952.1:n.*1023A>G
ENST00000682549.1:c.902A>G ENSP00000507483.1:p.Glu301Gly
ENST00000682932.1:c.877A>G ENSP00000507414.1:p.Lys293Glu
ENST00000683173.1:c.*998A>G ENSP00000508032.1:n.*998A>G
ENST00000683221.1:c.877A>G ENSP00000508093.1:p.Lys293Glu
ENST00000683401.1:n.810A>G
ENST00000683412.1:c.877A>G ENSP00000507538.1:p.Lys293Glu
ENST00000683462.1:c.902A>G ENSP00000507170.1:p.Glu301Gly
ENST00000683634.1:c.*998A>G ENSP00000507087.1:n.*998A>G
ENST00000683706.1:c.281A>G ENSP00000506745.1:p.Glu94Gly
ENST00000683916.1:c.902A>G ENSP00000508106.1:p.Glu301Gly
ENST00000684289.1:c.*552A>G ENSP00000506748.1:n.*552A>G
ENST00000684386.1:c.*91A>G ENSP00000507611.1:n.*91A>G
ENST00000356736.5:c.877A>G MANE Select ENSP00000349174.4:p.Lys293Glu
ENST00000356736.4:c.877A>G ENSP00000349174.4:p.Lys293Glu
ENST00000394833.6:c.877A>G ENSP00000378310.2:p.Lys293Glu
ENST00000424970.6:c.877A>G ENSP00000394548.2:p.Lys293Glu
NM_001135146.1:c.877A>G NP_001128618.1:p.Lys293Glu
NM_001135147.1:c.877A>G NP_001128619.1:p.Lys293Glu
NM_001135148.1:c.676A>G NP_001128620.1:p.Lys226Glu
NM_022154.5:c.877A>G NP_071437.3:p.Lys293Glu
XM_005263177.1:c.877A>G XP_005263234.1:p.Lys293Glu
XM_011532182.1:c.235A>G XP_011530484.1:p.Lys79Glu
XM_005263177.2:c.877A>G XP_005263234.1:p.Lys293Glu
XM_017008541.1:c.676A>G XP_016864030.1:p.Lys226Glu
XM_024454184.1:c.877A>G XP_024309952.1:p.Lys293Glu
NM_001135146.2:c.877A>G MANE Select NP_001128618.1:p.Lys293Glu
NM_001135148.2:c.676A>G NP_001128620.1:p.Lys226Glu