Canonical Allele Identifier: CA1922020008

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79085823T= , CM000672.2:g.79085823T=	GRCh38
NC_000010.10:g.80845580T= , CM000672.1:g.80845580T=	GRCh37
NC_000010.9:g.80515586T=	NCBI36
NG_028289.1:g.21789T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.-337+16553T= MANE Select	ENSP00000334474.5:n.-337+16553T=
ENST00000334512.9:c.-337+16553T=	ENSP00000334474.5:n.-337+16553T=
NM_020338.3:c.-337+16553T=	NP_065071.1:n.-337+16553T=
XM_005269988.2:c.-337+16553T=	XP_005270045.1:n.-337+16553T=
XM_006717923.2:c.-334+16553T=	XP_006717986.1:n.-334+16553T=
XM_006717924.2:c.-256+16553T=	XP_006717987.1:n.-256+16553T=
XM_006717925.2:c.-337+16553T=	XP_006717988.1:n.-337+16553T=
XM_005269988.3:c.-337+16553T=	XP_005270045.1:n.-337+16553T=
XM_006717923.3:c.-334+16553T=	XP_006717986.1:n.-334+16553T=
XM_006717924.3:c.-256+16553T=	XP_006717987.1:n.-256+16553T=
XM_006717925.3:c.-337+16553T=	XP_006717988.1:n.-337+16553T=
NM_020338.4:c.-337+16553T= MANE Select	NP_065071.1:n.-337+16553T=