Canonical Allele Identifier: CA413031390

Gene: ZNF674

Linked Data

• MyVariant Identifiers: chrX:g.46360677T>G (hg19) ; chrX:g.46501242T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501242T>G , CM000685.2:g.46501242T>G	GRCh38
NC_000023.10:g.46360677T>G , CM000685.1:g.46360677T>G	GRCh37
NC_000023.9:g.46245621T>G	NCBI36
NG_023376.1:g.49216A>C
NG_023376.2:g.49216A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683375.1:c.332A>C MANE Select	ENSP00000506769.1:p.Lys111Thr
ENST00000414387.6:c.329A>C	ENSP00000428248.1:p.Lys110Thr
ENST00000523374.5:c.347A>C	ENSP00000429148.1:p.Lys116Thr
NM_001039891.2:c.347A>C	NP_001034980.1:p.Lys116Thr
NM_001146291.1:c.329A>C	NP_001139763.1:p.Lys110Thr
NM_001190417.1:c.332A>C	NP_001177346.1:p.Lys111Thr
XM_011543941.1:c.347A>C	XP_011542243.1:p.Lys116Thr
XM_011543942.1:c.347A>C	XP_011542244.1:p.Lys116Thr
XM_011543943.1:c.344A>C	XP_011542245.1:p.Lys115Thr
XM_011543944.1:c.239A>C	XP_011542246.1:p.Lys80Thr
XM_011543945.1:c.146A>C	XP_011542247.1:p.Lys49Thr
XM_011543946.1:c.143A>C	XP_011542248.1:p.Lys48Thr
XM_011543941.3:c.347A>C	XP_011542243.1:p.Lys116Thr
XM_011543943.3:c.344A>C	XP_011542245.1:p.Lys115Thr
XM_011543944.2:c.239A>C	XP_011542246.1:p.Lys80Thr
XM_011543945.2:c.146A>C	XP_011542247.1:p.Lys49Thr
XM_017029728.1:c.146A>C	XP_016885217.1:p.Lys49Thr
XM_017029729.1:c.146A>C	XP_016885218.1:p.Lys49Thr
XM_017029730.2:c.146A>C	XP_016885219.1:p.Lys49Thr
XM_017029731.1:c.146A>C	XP_016885220.1:p.Lys49Thr
XM_017029732.1:c.143A>C	XP_016885221.1:p.Lys48Thr
XM_017029733.2:c.143A>C	XP_016885222.1:p.Lys48Thr
NM_001039891.3:c.347A>C	NP_001034980.1:p.Lys116Thr
NM_001146291.2:c.329A>C	NP_001139763.1:p.Lys110Thr
NM_001190417.2:c.332A>C MANE Select	NP_001177346.1:p.Lys111Thr