Canonical Allele Identifier: CA2427618949

Gene: ZNF674

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501237C= , CM000685.2:g.46501237C=	GRCh38
NC_000023.10:g.46360672C= , CM000685.1:g.46360672C=	GRCh37
NC_000023.9:g.46245616C=	NCBI36
NG_023376.1:g.49221G=
NG_023376.2:g.49221G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001190417.2:c.337G= MANE Select	NP_001177346.1:p.Glu113=
ENST00000683375.1:c.337G= MANE Select	ENSP00000506769.1:p.Glu113=
NM_001039891.2:c.352G=	NP_001034980.1:p.Glu118=
NM_001039891.3:c.352G=	NP_001034980.1:p.Glu118=
NM_001146291.1:c.334G=	NP_001139763.1:p.Glu112=
NM_001146291.2:c.334G=	NP_001139763.1:p.Glu112=
NM_001190417.1:c.337G=	NP_001177346.1:p.Glu113=
ENST00000414387.6:c.334G=	ENSP00000428248.1:p.Glu112=
ENST00000523374.5:c.352G=	ENSP00000429148.1:p.Glu118=
XM_011543941.1:c.352G=	XP_011542243.1:p.Glu118=
XM_011543941.3:c.352G=	XP_011542243.1:p.Glu118=
XM_011543942.1:c.352G=	XP_011542244.1:p.Glu118=
XM_011543943.1:c.349G=	XP_011542245.1:p.Glu117=
XM_011543943.3:c.349G=	XP_011542245.1:p.Glu117=
XM_011543944.1:c.244G=	XP_011542246.1:p.Glu82=
XM_011543944.2:c.244G=	XP_011542246.1:p.Glu82=
XM_011543945.1:c.151G=	XP_011542247.1:p.Glu51=
XM_011543945.2:c.151G=	XP_011542247.1:p.Glu51=
XM_011543946.1:c.148G=	XP_011542248.1:p.Glu50=
XM_017029728.1:c.151G=	XP_016885217.1:p.Glu51=
XM_017029729.1:c.151G=	XP_016885218.1:p.Glu51=
XM_017029730.2:c.151G=	XP_016885219.1:p.Glu51=
XM_017029731.1:c.151G=	XP_016885220.1:p.Glu51=
XM_017029732.1:c.148G=	XP_016885221.1:p.Glu50=
XM_017029733.2:c.148G=	XP_016885222.1:p.Glu50=