Canonical Allele Identifier: CA413031176

Gene: ZNF674

Linked Data

• MyVariant Identifiers: chrX:g.46360587T>C (hg19) ; chrX:g.46501152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501152T>C , CM000685.2:g.46501152T>C	GRCh38
NC_000023.10:g.46360587T>C , CM000685.1:g.46360587T>C	GRCh37
NC_000023.9:g.46245531T>C	NCBI36
NG_023376.1:g.49306A>G
NG_023376.2:g.49306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683375.1:c.422A>G MANE Select	ENSP00000506769.1:p.Tyr141Cys
ENST00000414387.6:c.419A>G	ENSP00000428248.1:p.Tyr140Cys
ENST00000523374.5:c.437A>G	ENSP00000429148.1:p.Tyr146Cys
NM_001039891.2:c.437A>G	NP_001034980.1:p.Tyr146Cys
NM_001146291.1:c.419A>G	NP_001139763.1:p.Tyr140Cys
NM_001190417.1:c.422A>G	NP_001177346.1:p.Tyr141Cys
XM_011543941.1:c.437A>G	XP_011542243.1:p.Tyr146Cys
XM_011543942.1:c.437A>G	XP_011542244.1:p.Tyr146Cys
XM_011543943.1:c.434A>G	XP_011542245.1:p.Tyr145Cys
XM_011543944.1:c.329A>G	XP_011542246.1:p.Tyr110Cys
XM_011543945.1:c.236A>G	XP_011542247.1:p.Tyr79Cys
XM_011543946.1:c.233A>G	XP_011542248.1:p.Tyr78Cys
XM_011543941.3:c.437A>G	XP_011542243.1:p.Tyr146Cys
XM_011543943.3:c.434A>G	XP_011542245.1:p.Tyr145Cys
XM_011543944.2:c.329A>G	XP_011542246.1:p.Tyr110Cys
XM_011543945.2:c.236A>G	XP_011542247.1:p.Tyr79Cys
XM_017029728.1:c.236A>G	XP_016885217.1:p.Tyr79Cys
XM_017029729.1:c.236A>G	XP_016885218.1:p.Tyr79Cys
XM_017029730.2:c.236A>G	XP_016885219.1:p.Tyr79Cys
XM_017029731.1:c.236A>G	XP_016885220.1:p.Tyr79Cys
XM_017029732.1:c.233A>G	XP_016885221.1:p.Tyr78Cys
XM_017029733.2:c.233A>G	XP_016885222.1:p.Tyr78Cys
NM_001039891.3:c.437A>G	NP_001034980.1:p.Tyr146Cys
NM_001146291.2:c.419A>G	NP_001139763.1:p.Tyr140Cys
NM_001190417.2:c.422A>G MANE Select	NP_001177346.1:p.Tyr141Cys