Canonical Allele Identifier: CA413031415
Gene: ZNF674 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46501254T>G , CM000685.2:g.46501254T>G GRCh38
NC_000023.10:g.46360689T>G , CM000685.1:g.46360689T>G GRCh37
NC_000023.9:g.46245633T>G NCBI36
NG_023376.1:g.49204A>C
NG_023376.2:g.49204A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683375.1:c.320A>C MANE Select ENSP00000506769.1:p.Lys107Thr
ENST00000414387.6:c.317A>C ENSP00000428248.1:p.Lys106Thr
ENST00000523374.5:c.335A>C ENSP00000429148.1:p.Lys112Thr
NM_001039891.2:c.335A>C NP_001034980.1:p.Lys112Thr
NM_001146291.1:c.317A>C NP_001139763.1:p.Lys106Thr
NM_001190417.1:c.320A>C NP_001177346.1:p.Lys107Thr
XM_011543941.1:c.335A>C XP_011542243.1:p.Lys112Thr
XM_011543942.1:c.335A>C XP_011542244.1:p.Lys112Thr
XM_011543943.1:c.332A>C XP_011542245.1:p.Lys111Thr
XM_011543944.1:c.227A>C XP_011542246.1:p.Lys76Thr
XM_011543945.1:c.134A>C XP_011542247.1:p.Lys45Thr
XM_011543946.1:c.131A>C XP_011542248.1:p.Lys44Thr
XM_011543941.3:c.335A>C XP_011542243.1:p.Lys112Thr
XM_011543943.3:c.332A>C XP_011542245.1:p.Lys111Thr
XM_011543944.2:c.227A>C XP_011542246.1:p.Lys76Thr
XM_011543945.2:c.134A>C XP_011542247.1:p.Lys45Thr
XM_017029728.1:c.134A>C XP_016885217.1:p.Lys45Thr
XM_017029729.1:c.134A>C XP_016885218.1:p.Lys45Thr
XM_017029730.2:c.134A>C XP_016885219.1:p.Lys45Thr
XM_017029731.1:c.134A>C XP_016885220.1:p.Lys45Thr
XM_017029732.1:c.131A>C XP_016885221.1:p.Lys44Thr
XM_017029733.2:c.131A>C XP_016885222.1:p.Lys44Thr
NM_001039891.3:c.335A>C NP_001034980.1:p.Lys112Thr
NM_001146291.2:c.317A>C NP_001139763.1:p.Lys106Thr
NM_001190417.2:c.320A>C MANE Select NP_001177346.1:p.Lys107Thr