Canonical Allele Identifier: CA14356767
Gene: ZNF423 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49796293A>G , CM000678.2:g.49796293A>G GRCh38
NC_000016.9:g.49830204A>G , CM000678.1:g.49830204A>G GRCh37
NC_000016.8:g.48387705A>G NCBI36
NG_032972.1:g.66627T>C
NG_032972.2:g.66627T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000563137.7:c.41-6747T>C MANE Select ENSP00000455588.3:n.41-6747T>C
ENST00000262383.6:c.17-6747T>C ENSP00000262383.2:n.17-6747T>C
ENST00000561648.5:c.17-6747T>C ENSP00000455426.1:n.17-6747T>C
ENST00000562520.1:c.-164-6747T>C ENSP00000457664.1:n.-164-6747T>C
ENST00000563137.6:c.-164-6747T>C ENSP00000455588.2:n.-164-6747T>C
NM_001271620.1:c.-164-6747T>C NP_001258549.1:n.-164-6747T>C
NM_015069.3:c.17-6747T>C NP_055884.2:n.17-6747T>C
XM_006721171.2:c.62-6747T>C XP_006721234.1:n.62-6747T>C
XM_011522962.1:c.110-6747T>C XP_011521264.1:n.110-6747T>C
NM_001271620.2:c.-164-6747T>C NP_001258549.1:n.-164-6747T>C
NM_015069.4:c.17-6747T>C NP_055884.2:n.17-6747T>C
XM_006721171.4:c.62-6747T>C XP_006721234.1:n.62-6747T>C
XM_017023076.2:c.41-6747T>C XP_016878565.1:n.41-6747T>C
NM_001379286.1:c.41-6747T>C MANE Select NP_001366215.1:n.41-6747T>C
NM_015069.5:c.17-6747T>C NP_055884.2:n.17-6747T>C
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