Canonical Allele Identifier: CA14225249

Gene: ZFHX3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72945475C>T , CM000678.2:g.72945475C>T	GRCh38
NC_000016.9:g.72979374C>T , CM000678.1:g.72979374C>T	GRCh37
NC_000016.8:g.71536875C>T	NCBI36
NG_013211.1:g.118161G>A
NG_013211.2:g.951457G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268489.10:c.3216+4994G>A MANE Select	ENSP00000268489.5:n.3216+4994G>A
ENST00000641206.2:c.3216+4994G>A	ENSP00000493252.1:n.3216+4994G>A
ENST00000268489.9:c.3216+4994G>A	ENSP00000268489.5:n.3216+4994G>A
ENST00000397992.5:c.474+4994G>A	ENSP00000438926.3:n.474+4994G>A
NM_001164766.1:c.474+4994G>A	NP_001158238.1:n.474+4994G>A
NM_006885.3:c.3216+4994G>A	NP_008816.3:n.3216+4994G>A
XM_005255957.2:c.3216+4994G>A	XP_005256014.1:n.3216+4994G>A
XM_005255957.4:c.3216+4994G>A	XP_005256014.1:n.3216+4994G>A
XM_017023251.2:c.567+4994G>A	XP_016878740.1:n.567+4994G>A
XM_024450291.1:c.567+4994G>A	XP_024306059.1:n.567+4994G>A
NM_006885.4:c.3216+4994G>A MANE Select	NP_008816.3:n.3216+4994G>A
NM_001164766.2:c.474+4994G>A	NP_001158238.1:n.474+4994G>A
NM_001386735.1:c.3216+4994G>A	NP_001373664.1:n.3216+4994G>A