Canonical Allele Identifier: CA1795296518

Gene: ZFHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864205T= , CM000670.2:g.76864205T=	GRCh38
NC_000008.10:g.77776441T= , CM000670.1:g.77776441T=	GRCh37
NC_000008.9:g.77938996T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10491T= MANE Select	ENSP00000498627.1:p.Pro3497=
ENST00000518282.5:c.10413T=	ENSP00000430848.1:p.Pro3471=
ENST00000521891.6:c.10491T=	ENSP00000430497.2:p.Pro3497=
NM_024721.4:c.10491T=	NP_078997.4:p.Pro3497=
XM_011517592.1:c.10491T=	XP_011515894.1:p.Pro3497=
XM_011517593.1:c.10491T=	XP_011515895.1:p.Pro3497=
XM_011517594.1:c.10491T=	XP_011515896.1:p.Pro3497=
XM_011517595.1:c.10491T=	XP_011515897.1:p.Pro3497=
XM_011517596.1:c.10413T=	XP_011515898.1:p.Pro3471=
XM_011517597.1:c.10374T=	XP_011515899.1:p.Pro3458=
XM_011517592.3:c.10491T=	XP_011515894.1:p.Pro3497=
XM_011517593.2:c.10491T=	XP_011515895.1:p.Pro3497=
XM_011517594.2:c.10491T=	XP_011515896.1:p.Pro3497=
XM_011517595.2:c.10491T=	XP_011515897.1:p.Pro3497=
XM_011517596.2:c.10413T=	XP_011515898.1:p.Pro3471=
XM_011517597.2:c.10374T=	XP_011515899.1:p.Pro3458=
XM_017013845.1:c.10296T=	XP_016869334.1:p.Pro3432=
NM_024721.5:c.10491T= MANE Select	NP_078997.4:p.Pro3497=