Canonical Allele Identifier: CA1432667976
Gene: ZNF732 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288669G= , CM000666.2:g.288669G= GRCh38
NC_000004.11:g.282458G= , CM000666.1:g.282458G= GRCh37
NC_000004.10:g.272458G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6769C= MANE Select ENSP00000415774.1:n.226+6769C=
ENST00000419098.5:c.226+6769C= ENSP00000415774.1:n.226+6769C=
ENST00000619749.1:c.223+6769C= ENSP00000478210.1:n.223+6769C=
NM_001137608.1:c.226+6769C= NP_001131080.1:n.226+6769C=
NM_001137608.2:c.226+6769C= NP_001131080.1:n.226+6769C=
NM_001137608.3:c.226+6769C= MANE Select NP_001131080.1:n.226+6769C=
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