Canonical Allele Identifier: CA1922126869

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79307723C= , CM000672.2:g.79307723C=	GRCh38
NC_000010.10:g.81067480C= , CM000672.1:g.81067480C=	GRCh37
NC_000010.9:g.80737486C=	NCBI36
NG_028289.1:g.243689C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020338.4:c.2835+152C= MANE Select	NP_065071.1:n.2835+152C=
ENST00000334512.10:c.2835+152C= MANE Select	ENSP00000334474.5:n.2835+152C=
NM_020338.3:c.2835+152C=	NP_065071.1:n.2835+152C=
ENST00000334512.9:c.2835+152C=	ENSP00000334474.5:n.2835+152C=
ENST00000446377.3:c.2538+152C=	ENSP00000401558.3:n.2538+152C=
ENST00000611351.1:c.459-6331C=	ENSP00000481736.1:n.459-6331C=
XM_005269987.3:c.2853+152C=	XP_005270044.1:n.2853+152C=
XM_005269987.5:c.2853+152C=	XP_005270044.1:n.2853+152C=
XM_005269988.2:c.2853+152C=	XP_005270045.1:n.2853+152C=
XM_005269988.3:c.2853+152C=	XP_005270045.1:n.2853+152C=
XM_006717923.2:c.2853+152C=	XP_006717986.1:n.2853+152C=
XM_006717923.3:c.2853+152C=	XP_006717986.1:n.2853+152C=
XM_006717924.2:c.2853+152C=	XP_006717987.1:n.2853+152C=
XM_006717924.3:c.2853+152C=	XP_006717987.1:n.2853+152C=
XM_006717925.2:c.2853+152C=	XP_006717988.1:n.2853+152C=
XM_006717925.3:c.2853+152C=	XP_006717988.1:n.2853+152C=
XM_011539978.1:c.2481+152C=	XP_011538280.1:n.2481+152C=
XM_011539978.2:c.2481+152C=	XP_011538280.1:n.2481+152C=
XM_011539979.1:c.2481+152C=	XP_011538281.1:n.2481+152C=
XM_011539980.1:c.2463+152C=	XP_011538282.1:n.2463+152C=
XM_011539980.3:c.2463+152C=	XP_011538282.1:n.2463+152C=
XM_017016440.2:c.2700+152C=	XP_016871929.1:n.2700+152C=
XM_017016441.1:c.2481+152C=	XP_016871930.1:n.2481+152C=
XM_017016442.1:c.2463+152C=	XP_016871931.1:n.2463+152C=
XM_017016443.1:c.2481+152C=	XP_016871932.1:n.2481+152C=