Canonical Allele Identifier: CA1922101287

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79256182T= , CM000672.2:g.79256182T=	GRCh38
NC_000010.10:g.81015939T= , CM000672.1:g.81015939T=	GRCh37
NC_000010.9:g.80685945T=	NCBI36
NG_028289.1:g.192148T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.281-20999T= MANE Select	ENSP00000334474.5:n.281-20999T=
ENST00000334512.9:c.281-20999T=	ENSP00000334474.5:n.281-20999T=
ENST00000472035.5:n.70+12444T=
ENST00000611351.1:c.281-20999T=	ENSP00000481736.1:n.281-20999T=
NM_020338.3:c.281-20999T=	NP_065071.1:n.281-20999T=
XM_005269987.3:c.281-20999T=	XP_005270044.1:n.281-20999T=
XM_005269988.2:c.281-20999T=	XP_005270045.1:n.281-20999T=
XM_006717923.2:c.281-20999T=	XP_006717986.1:n.281-20999T=
XM_006717924.2:c.281-20999T=	XP_006717987.1:n.281-20999T=
XM_006717925.2:c.281-20999T=	XP_006717988.1:n.281-20999T=
XM_011539978.1:c.-93+12444T=	XP_011538280.1:n.-93+12444T=
XM_011539979.1:c.-93+13213T=	XP_011538281.1:n.-93+13213T=
XM_011539980.1:c.-93+12444T=	XP_011538282.1:n.-93+12444T=
XM_005269987.5:c.281-20999T=	XP_005270044.1:n.281-20999T=
XM_005269988.3:c.281-20999T=	XP_005270045.1:n.281-20999T=
XM_006717923.3:c.281-20999T=	XP_006717986.1:n.281-20999T=
XM_006717924.3:c.281-20999T=	XP_006717987.1:n.281-20999T=
XM_006717925.3:c.281-20999T=	XP_006717988.1:n.281-20999T=
XM_011539978.2:c.-93+12444T=	XP_011538280.1:n.-93+12444T=
XM_011539980.3:c.-93+12444T=	XP_011538282.1:n.-93+12444T=
XM_017016441.1:c.-93+13112T=	XP_016871930.1:n.-93+13112T=
XM_017016442.1:c.-93+13213T=	XP_016871931.1:n.-93+13213T=
XM_017016443.1:c.-93+13288T=	XP_016871932.1:n.-93+13288T=
NM_020338.4:c.281-20999T= MANE Select	NP_065071.1:n.281-20999T=