Canonical Allele Identifier: CA2232016914

Gene: ZFHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72975125A= , CM000678.2:g.72975125A=	GRCh38
NC_000016.9:g.73009024A= , CM000678.1:g.73009024A=	GRCh37
NC_000016.8:g.71566525A=	NCBI36
NG_013211.1:g.88511T=
NG_013211.2:g.921807T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006885.4:c.-49-14931T= MANE Select	NP_008816.3:n.-49-14931T=
ENST00000268489.10:c.-49-14931T= MANE Select	ENSP00000268489.5:n.-49-14931T=
NM_001164766.1:c.-23-24160T=	NP_001158238.1:n.-23-24160T=
NM_001164766.2:c.-23-24160T=	NP_001158238.1:n.-23-24160T=
NM_001386735.1:c.-49-14931T=	NP_001373664.1:n.-49-14931T=
NM_006885.3:c.-49-14931T=	NP_008816.3:n.-49-14931T=
ENST00000268489.9:c.-49-14931T=	ENSP00000268489.5:n.-49-14931T=
ENST00000397992.5:c.-23-24160T=	ENSP00000438926.3:n.-23-24160T=
ENST00000641206.2:c.-49-14931T=	ENSP00000493252.1:n.-49-14931T=
XM_005255957.2:c.-49-14931T=	XP_005256014.1:n.-49-14931T=
XM_005255957.4:c.-49-14931T=	XP_005256014.1:n.-49-14931T=
XM_017023251.2:c.71-24160T=	XP_016878740.1:n.71-24160T=
XM_024450291.1:c.71-24160T=	XP_024306059.1:n.71-24160T=