Canonical Allele Identifier: CA14225211

Gene: ZFHX3

Genomic Alleles

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

Transcript Alleles

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