Canonical Allele Identifier: CA1795217184
Gene: ZFHX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.76699390A>T , CM000670.2:g.76699390A>T GRCh38
NC_000008.10:g.77611625A>T , CM000670.1:g.77611625A>T GRCh37
NC_000008.9:g.77774180A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523885.2:c.-46-4653A>T ENSP00000429495.2:n.-46-4653A>T
ENST00000651372.2:c.-46-4653A>T MANE Select ENSP00000498627.1:n.-46-4653A>T
ENST00000458716.2:n.342-4653A>T
ENST00000517585.1:c.-46-4653A>T ENSP00000427775.1:n.-46-4653A>T
ENST00000517683.1:n.382+17770A>T
ENST00000520307.5:c.-46-4653A>T ENSP00000428525.1:n.-46-4653A>T
ENST00000521891.6:c.-46-4653A>T ENSP00000430497.2:n.-46-4653A>T
ENST00000523809.1:c.-67-4208A>T ENSP00000427739.1:n.-67-4208A>T
ENST00000523885.1:c.-46-4653A>T ENSP00000429495.1:n.-46-4653A>T
NM_024721.4:c.-46-4653A>T NP_078997.4:n.-46-4653A>T
XM_011517592.1:c.-46-4653A>T XP_011515894.1:n.-46-4653A>T
XM_011517593.1:c.-67-4208A>T XP_011515895.1:n.-67-4208A>T
XM_011517594.1:c.-46-4653A>T XP_011515896.1:n.-46-4653A>T
XM_011517595.1:c.-46-4653A>T XP_011515897.1:n.-46-4653A>T
XM_011517596.1:c.-46-4653A>T XP_011515898.1:n.-46-4653A>T
XM_011517597.1:c.-46-4653A>T XP_011515899.1:n.-46-4653A>T
XM_011517592.3:c.-46-4653A>T XP_011515894.1:n.-46-4653A>T
XM_011517593.2:c.-67-4208A>T XP_011515895.1:n.-67-4208A>T
XM_011517594.2:c.-46-4653A>T XP_011515896.1:n.-46-4653A>T
XM_011517595.2:c.-46-4653A>T XP_011515897.1:n.-46-4653A>T
XM_011517596.2:c.-46-4653A>T XP_011515898.1:n.-46-4653A>T
XM_011517597.2:c.-46-4653A>T XP_011515899.1:n.-46-4653A>T
XM_017013845.1:c.-46-4653A>T XP_016869334.1:n.-46-4653A>T
NM_024721.5:c.-46-4653A>T MANE Select NP_078997.4:n.-46-4653A>T