Canonical Allele Identifier: CA2830545182
Gene: ZFHX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.76864293_76864294insAGACG , CM000670.2:g.76864293_76864294insAGACG GRCh38
NC_000008.10:g.77776529_77776530insAGACG , CM000670.1:g.77776529_77776530insAGACG GRCh37
NC_000008.9:g.77939084_77939085insAGACG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651372.2:c.10579_10580insAGACG MANE Select ENSP00000498627.1:p.Pro3527GlnfsTer?
ENST00000518282.5:c.10501_10502insAGACG ENSP00000430848.1:p.Pro3501GlnfsTer?
ENST00000521891.6:c.10579_10580insAGACG ENSP00000430497.2:p.Pro3527GlnfsTer?
NM_024721.4:c.10579_10580insAGACG NP_078997.4:p.Pro3527GlnfsTer?
XM_011517592.1:c.10579_10580insAGACG XP_011515894.1:p.Pro3527GlnfsTer?
XM_011517593.1:c.10579_10580insAGACG XP_011515895.1:p.Pro3527GlnfsTer?
XM_011517594.1:c.10579_10580insAGACG XP_011515896.1:p.Pro3527GlnfsTer?
XM_011517595.1:c.10579_10580insAGACG XP_011515897.1:p.Pro3527GlnfsTer?
XM_011517596.1:c.10501_10502insAGACG XP_011515898.1:p.Pro3501GlnfsTer?
XM_011517597.1:c.10462_10463insAGACG XP_011515899.1:p.Pro3488GlnfsTer?
XM_011517592.3:c.10579_10580insAGACG XP_011515894.1:p.Pro3527GlnfsTer?
XM_011517593.2:c.10579_10580insAGACG XP_011515895.1:p.Pro3527GlnfsTer?
XM_011517594.2:c.10579_10580insAGACG XP_011515896.1:p.Pro3527GlnfsTer?
XM_011517595.2:c.10579_10580insAGACG XP_011515897.1:p.Pro3527GlnfsTer?
XM_011517596.2:c.10501_10502insAGACG XP_011515898.1:p.Pro3501GlnfsTer?
XM_011517597.2:c.10462_10463insAGACG XP_011515899.1:p.Pro3488GlnfsTer?
XM_017013845.1:c.10384_10385insAGACG XP_016869334.1:p.Pro3462GlnfsTer?
NM_024721.5:c.10579_10580insAGACG MANE Select NP_078997.4:p.Pro3527GlnfsTer?