Canonical Allele Identifier: CA13196145

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79200216T>C , CM000672.2:g.79200216T>C	GRCh38
NC_000010.10:g.80959973T>C , CM000672.1:g.80959973T>C	GRCh37
NC_000010.9:g.80629979T>C	NCBI36
NG_028289.1:g.136182T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020338.4:c.-49-1368T>C MANE Select	NP_065071.1:n.-49-1368T>C
ENST00000334512.10:c.-49-1368T>C MANE Select	ENSP00000334474.5:n.-49-1368T>C
NM_020338.3:c.-49-1368T>C	NP_065071.1:n.-49-1368T>C
ENST00000334512.9:c.-49-1368T>C	ENSP00000334474.5:n.-49-1368T>C
XM_005269987.3:c.-49-1368T>C	XP_005270044.1:n.-49-1368T>C
XM_005269987.5:c.-49-1368T>C	XP_005270044.1:n.-49-1368T>C
XM_005269988.2:c.-49-1368T>C	XP_005270045.1:n.-49-1368T>C
XM_005269988.3:c.-49-1368T>C	XP_005270045.1:n.-49-1368T>C
XM_006717923.2:c.-49-1368T>C	XP_006717986.1:n.-49-1368T>C
XM_006717923.3:c.-49-1368T>C	XP_006717986.1:n.-49-1368T>C
XM_006717924.2:c.-49-1368T>C	XP_006717987.1:n.-49-1368T>C
XM_006717924.3:c.-49-1368T>C	XP_006717987.1:n.-49-1368T>C
XM_006717925.2:c.-49-1368T>C	XP_006717988.1:n.-49-1368T>C
XM_006717925.3:c.-49-1368T>C	XP_006717988.1:n.-49-1368T>C