Canonical Allele Identifier: CA1922019959

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79085736C= , CM000672.2:g.79085736C=	GRCh38
NC_000010.10:g.80845493C= , CM000672.1:g.80845493C=	GRCh37
NC_000010.9:g.80515499C=	NCBI36
NG_028289.1:g.21702C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.-337+16466C= MANE Select	ENSP00000334474.5:n.-337+16466C=
ENST00000334512.9:c.-337+16466C=	ENSP00000334474.5:n.-337+16466C=
NM_020338.3:c.-337+16466C=	NP_065071.1:n.-337+16466C=
XM_005269988.2:c.-337+16466C=	XP_005270045.1:n.-337+16466C=
XM_006717923.2:c.-334+16466C=	XP_006717986.1:n.-334+16466C=
XM_006717924.2:c.-256+16466C=	XP_006717987.1:n.-256+16466C=
XM_006717925.2:c.-337+16466C=	XP_006717988.1:n.-337+16466C=
XM_005269988.3:c.-337+16466C=	XP_005270045.1:n.-337+16466C=
XM_006717923.3:c.-334+16466C=	XP_006717986.1:n.-334+16466C=
XM_006717924.3:c.-256+16466C=	XP_006717987.1:n.-256+16466C=
XM_006717925.3:c.-337+16466C=	XP_006717988.1:n.-337+16466C=
NM_020338.4:c.-337+16466C= MANE Select	NP_065071.1:n.-337+16466C=