Canonical Allele Identifier: CA516369435
Gene: ZNF674 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.46360691G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46501256G>A , CM000685.2:g.46501256G>A GRCh38
NC_000023.10:g.46360691G>A , CM000685.1:g.46360691G>A GRCh37
NC_000023.9:g.46245635G>A NCBI36
NG_023376.1:g.49202C>T
NG_023376.2:g.49202C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683375.1:c.318C>T MANE Select ENSP00000506769.1:p.Gly106=
ENST00000414387.6:c.315C>T ENSP00000428248.1:p.Gly105=
ENST00000523374.5:c.333C>T ENSP00000429148.1:p.Gly111=
NM_001039891.2:c.333C>T NP_001034980.1:p.Gly111=
NM_001146291.1:c.315C>T NP_001139763.1:p.Gly105=
NM_001190417.1:c.318C>T NP_001177346.1:p.Gly106=
XM_011543941.1:c.333C>T XP_011542243.1:p.Gly111=
XM_011543942.1:c.333C>T XP_011542244.1:p.Gly111=
XM_011543943.1:c.330C>T XP_011542245.1:p.Gly110=
XM_011543944.1:c.225C>T XP_011542246.1:p.Gly75=
XM_011543945.1:c.132C>T XP_011542247.1:p.Gly44=
XM_011543946.1:c.129C>T XP_011542248.1:p.Gly43=
XM_011543941.3:c.333C>T XP_011542243.1:p.Gly111=
XM_011543943.3:c.330C>T XP_011542245.1:p.Gly110=
XM_011543944.2:c.225C>T XP_011542246.1:p.Gly75=
XM_011543945.2:c.132C>T XP_011542247.1:p.Gly44=
XM_017029728.1:c.132C>T XP_016885217.1:p.Gly44=
XM_017029729.1:c.132C>T XP_016885218.1:p.Gly44=
XM_017029730.2:c.132C>T XP_016885219.1:p.Gly44=
XM_017029731.1:c.132C>T XP_016885220.1:p.Gly44=
XM_017029732.1:c.129C>T XP_016885221.1:p.Gly43=
XM_017029733.2:c.129C>T XP_016885222.1:p.Gly43=
NM_001039891.3:c.333C>T NP_001034980.1:p.Gly111=
NM_001146291.2:c.315C>T NP_001139763.1:p.Gly105=
NM_001190417.2:c.318C>T MANE Select NP_001177346.1:p.Gly106=