Canonical Allele Identifier: CA723592024

Gene: ZFHX3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72995261T>A , CM000678.2:g.72995261T>A	GRCh38
NC_000016.9:g.73029160T>A , CM000678.1:g.73029160T>A	GRCh37
NC_000016.8:g.71586661T>A	NCBI36
NG_013211.1:g.68375A>T
NG_013211.2:g.901671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268489.10:c.-49-35067A>T MANE Select	ENSP00000268489.5:n.-49-35067A>T
ENST00000641206.2:c.-49-35067A>T	ENSP00000493252.1:n.-49-35067A>T
ENST00000268489.9:c.-49-35067A>T	ENSP00000268489.5:n.-49-35067A>T
ENST00000397992.5:c.-23-44296A>T	ENSP00000438926.3:n.-23-44296A>T
NM_001164766.1:c.-23-44296A>T	NP_001158238.1:n.-23-44296A>T
NM_006885.3:c.-49-35067A>T	NP_008816.3:n.-49-35067A>T
XM_005255957.2:c.-49-35067A>T	XP_005256014.1:n.-49-35067A>T
XM_005255957.4:c.-49-35067A>T	XP_005256014.1:n.-49-35067A>T
XM_017023251.2:c.71-44296A>T	XP_016878740.1:n.71-44296A>T
XM_024450291.1:c.71-44296A>T	XP_024306059.1:n.71-44296A>T
NM_006885.4:c.-49-35067A>T MANE Select	NP_008816.3:n.-49-35067A>T
NM_001164766.2:c.-23-44296A>T	NP_001158238.1:n.-23-44296A>T
NM_001386735.1:c.-49-35067A>T	NP_001373664.1:n.-49-35067A>T