Canonical Allele Identifier: CA1432667969
Gene: ZNF732 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288654C= , CM000666.2:g.288654C= GRCh38
NC_000004.11:g.282443C= , CM000666.1:g.282443C= GRCh37
NC_000004.10:g.272443C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6784G= MANE Select ENSP00000415774.1:n.226+6784G=
ENST00000419098.5:c.226+6784G= ENSP00000415774.1:n.226+6784G=
ENST00000619749.1:c.223+6784G= ENSP00000478210.1:n.223+6784G=
NM_001137608.1:c.226+6784G= NP_001131080.1:n.226+6784G=
NM_001137608.2:c.226+6784G= NP_001131080.1:n.226+6784G=
NM_001137608.3:c.226+6784G= MANE Select NP_001131080.1:n.226+6784G=
Search 100 bp 5'
Search 100 bp 3'