Canonical Allele Identifier: CA14285688
Gene: ZFHX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73034779G>A , CM000678.2:g.73034779G>A GRCh38
NC_000016.9:g.73068678G>A , CM000678.1:g.73068678G>A GRCh37
NC_000016.8:g.71626179G>A NCBI36
NG_013211.1:g.28857C>T
NG_013211.2:g.862153C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000268489.10:c.-50+12973C>T MANE Select ENSP00000268489.5:n.-50+12973C>T
ENST00000641206.2:c.-50+23751C>T ENSP00000493252.1:n.-50+23751C>T
ENST00000268489.9:c.-50+12973C>T ENSP00000268489.5:n.-50+12973C>T
ENST00000397992.5:c.-24+23751C>T ENSP00000438926.3:n.-24+23751C>T
NM_001164766.1:c.-24+23751C>T NP_001158238.1:n.-24+23751C>T
NM_006885.3:c.-50+12973C>T NP_008816.3:n.-50+12973C>T
XM_005255957.2:c.-50+12973C>T XP_005256014.1:n.-50+12973C>T
XM_005255957.4:c.-50+12973C>T XP_005256014.1:n.-50+12973C>T
XM_017023251.2:c.70+12973C>T XP_016878740.1:n.70+12973C>T
XM_024450291.1:c.70+12973C>T XP_024306059.1:n.70+12973C>T
NM_006885.4:c.-50+12973C>T MANE Select NP_008816.3:n.-50+12973C>T
NM_001164766.2:c.-24+23751C>T NP_001158238.1:n.-24+23751C>T
NM_001386735.1:c.-50+58456C>T NP_001373664.1:n.-50+58456C>T
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