Canonical Allele Identifier: CA2427618929

Gene: ZNF674

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501144A= , CM000685.2:g.46501144A=	GRCh38
NC_000023.10:g.46360579A= , CM000685.1:g.46360579A=	GRCh37
NC_000023.9:g.46245523A=	NCBI36
NG_023376.1:g.49314T=
NG_023376.2:g.49314T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683375.1:c.430T= MANE Select	ENSP00000506769.1:p.Trp144=
ENST00000414387.6:c.427T=	ENSP00000428248.1:p.Trp143=
ENST00000523374.5:c.445T=	ENSP00000429148.1:p.Trp149=
NM_001039891.2:c.445T=	NP_001034980.1:p.Trp149=
NM_001146291.1:c.427T=	NP_001139763.1:p.Trp143=
NM_001190417.1:c.430T=	NP_001177346.1:p.Trp144=
XM_011543941.1:c.445T=	XP_011542243.1:p.Trp149=
XM_011543942.1:c.445T=	XP_011542244.1:p.Trp149=
XM_011543943.1:c.442T=	XP_011542245.1:p.Trp148=
XM_011543944.1:c.337T=	XP_011542246.1:p.Trp113=
XM_011543945.1:c.244T=	XP_011542247.1:p.Trp82=
XM_011543946.1:c.241T=	XP_011542248.1:p.Trp81=
XM_011543941.3:c.445T=	XP_011542243.1:p.Trp149=
XM_011543943.3:c.442T=	XP_011542245.1:p.Trp148=
XM_011543944.2:c.337T=	XP_011542246.1:p.Trp113=
XM_011543945.2:c.244T=	XP_011542247.1:p.Trp82=
XM_017029728.1:c.244T=	XP_016885217.1:p.Trp82=
XM_017029729.1:c.244T=	XP_016885218.1:p.Trp82=
XM_017029730.2:c.244T=	XP_016885219.1:p.Trp82=
XM_017029731.1:c.244T=	XP_016885220.1:p.Trp82=
XM_017029732.1:c.241T=	XP_016885221.1:p.Trp81=
XM_017029733.2:c.241T=	XP_016885222.1:p.Trp81=
NM_001039891.3:c.445T=	NP_001034980.1:p.Trp149=
NM_001146291.2:c.427T=	NP_001139763.1:p.Trp143=
NM_001190417.2:c.430T= MANE Select	NP_001177346.1:p.Trp144=