Canonical Allele Identifier: CA2231974067
Gene: ZFHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72897186A>T , CM000678.2:g.72897186A>T GRCh38
NC_000016.9:g.72931085A>T , CM000678.1:g.72931085A>T GRCh37
NC_000016.8:g.71488586A>T NCBI36
NG_013211.1:g.166450T>A
NG_013211.2:g.999746T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268489.10:c.3217-7224T>A MANE Select ENSP00000268489.5:n.3217-7224T>A
ENST00000641206.2:c.3217-7224T>A ENSP00000493252.1:n.3217-7224T>A
ENST00000268489.9:c.3217-7224T>A ENSP00000268489.5:n.3217-7224T>A
ENST00000397992.5:c.475-7224T>A ENSP00000438926.3:n.475-7224T>A
NM_001164766.1:c.475-7224T>A NP_001158238.1:n.475-7224T>A
NM_006885.3:c.3217-7224T>A NP_008816.3:n.3217-7224T>A
XM_005255957.2:c.3217-7224T>A XP_005256014.1:n.3217-7224T>A
XM_005255957.4:c.3217-7224T>A XP_005256014.1:n.3217-7224T>A
XM_017023251.2:c.568-7224T>A XP_016878740.1:n.568-7224T>A
XM_024450291.1:c.568-7224T>A XP_024306059.1:n.568-7224T>A
NM_006885.4:c.3217-7224T>A MANE Select NP_008816.3:n.3217-7224T>A
NM_001164766.2:c.475-7224T>A NP_001158238.1:n.475-7224T>A
NM_001386735.1:c.3217-7224T>A NP_001373664.1:n.3217-7224T>A