Canonical Allele Identifier: CA413031180

Gene: ZNF674

Linked Data

• MyVariant Identifiers: chrX:g.46360588A>T (hg19) ; chrX:g.46501153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501153A>T , CM000685.2:g.46501153A>T	GRCh38
NC_000023.10:g.46360588A>T , CM000685.1:g.46360588A>T	GRCh37
NC_000023.9:g.46245532A>T	NCBI36
NG_023376.1:g.49305T>A
NG_023376.2:g.49305T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683375.1:c.421T>A MANE Select	ENSP00000506769.1:p.Tyr141Asn
ENST00000414387.6:c.418T>A	ENSP00000428248.1:p.Tyr140Asn
ENST00000523374.5:c.436T>A	ENSP00000429148.1:p.Tyr146Asn
NM_001039891.2:c.436T>A	NP_001034980.1:p.Tyr146Asn
NM_001146291.1:c.418T>A	NP_001139763.1:p.Tyr140Asn
NM_001190417.1:c.421T>A	NP_001177346.1:p.Tyr141Asn
XM_011543941.1:c.436T>A	XP_011542243.1:p.Tyr146Asn
XM_011543942.1:c.436T>A	XP_011542244.1:p.Tyr146Asn
XM_011543943.1:c.433T>A	XP_011542245.1:p.Tyr145Asn
XM_011543944.1:c.328T>A	XP_011542246.1:p.Tyr110Asn
XM_011543945.1:c.235T>A	XP_011542247.1:p.Tyr79Asn
XM_011543946.1:c.232T>A	XP_011542248.1:p.Tyr78Asn
XM_011543941.3:c.436T>A	XP_011542243.1:p.Tyr146Asn
XM_011543943.3:c.433T>A	XP_011542245.1:p.Tyr145Asn
XM_011543944.2:c.328T>A	XP_011542246.1:p.Tyr110Asn
XM_011543945.2:c.235T>A	XP_011542247.1:p.Tyr79Asn
XM_017029728.1:c.235T>A	XP_016885217.1:p.Tyr79Asn
XM_017029729.1:c.235T>A	XP_016885218.1:p.Tyr79Asn
XM_017029730.2:c.235T>A	XP_016885219.1:p.Tyr79Asn
XM_017029731.1:c.235T>A	XP_016885220.1:p.Tyr79Asn
XM_017029732.1:c.232T>A	XP_016885221.1:p.Tyr78Asn
XM_017029733.2:c.232T>A	XP_016885222.1:p.Tyr78Asn
NM_001039891.3:c.436T>A	NP_001034980.1:p.Tyr146Asn
NM_001146291.2:c.418T>A	NP_001139763.1:p.Tyr140Asn
NM_001190417.2:c.421T>A MANE Select	NP_001177346.1:p.Tyr141Asn