Canonical Allele Identifier: CA413031385

Gene: ZNF674

Linked Data

• MyVariant Identifiers: chrX:g.46360675C>G (hg19) ; chrX:g.46501240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46501240C>G , CM000685.2:g.46501240C>G	GRCh38
NC_000023.10:g.46360675C>G , CM000685.1:g.46360675C>G	GRCh37
NC_000023.9:g.46245619C>G	NCBI36
NG_023376.1:g.49218G>C
NG_023376.2:g.49218G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683375.1:c.334G>C MANE Select	ENSP00000506769.1:p.Asp112His
ENST00000414387.6:c.331G>C	ENSP00000428248.1:p.Asp111His
ENST00000523374.5:c.349G>C	ENSP00000429148.1:p.Asp117His
NM_001039891.2:c.349G>C	NP_001034980.1:p.Asp117His
NM_001146291.1:c.331G>C	NP_001139763.1:p.Asp111His
NM_001190417.1:c.334G>C	NP_001177346.1:p.Asp112His
XM_011543941.1:c.349G>C	XP_011542243.1:p.Asp117His
XM_011543942.1:c.349G>C	XP_011542244.1:p.Asp117His
XM_011543943.1:c.346G>C	XP_011542245.1:p.Asp116His
XM_011543944.1:c.241G>C	XP_011542246.1:p.Asp81His
XM_011543945.1:c.148G>C	XP_011542247.1:p.Asp50His
XM_011543946.1:c.145G>C	XP_011542248.1:p.Asp49His
XM_011543941.3:c.349G>C	XP_011542243.1:p.Asp117His
XM_011543943.3:c.346G>C	XP_011542245.1:p.Asp116His
XM_011543944.2:c.241G>C	XP_011542246.1:p.Asp81His
XM_011543945.2:c.148G>C	XP_011542247.1:p.Asp50His
XM_017029728.1:c.148G>C	XP_016885217.1:p.Asp50His
XM_017029729.1:c.148G>C	XP_016885218.1:p.Asp50His
XM_017029730.2:c.148G>C	XP_016885219.1:p.Asp50His
XM_017029731.1:c.148G>C	XP_016885220.1:p.Asp50His
XM_017029732.1:c.145G>C	XP_016885221.1:p.Asp49His
XM_017029733.2:c.145G>C	XP_016885222.1:p.Asp49His
NM_001039891.3:c.349G>C	NP_001034980.1:p.Asp117His
NM_001146291.2:c.331G>C	NP_001139763.1:p.Asp111His
NM_001190417.2:c.334G>C MANE Select	NP_001177346.1:p.Asp112His