Canonical Allele Identifier: CA13196137

Gene: ZMIZ1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79193379A>C , CM000672.2:g.79193379A>C	GRCh38
NC_000010.10:g.80953136A>C , CM000672.1:g.80953136A>C	GRCh37
NC_000010.9:g.80623142A>C	NCBI36
NG_028289.1:g.129345A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.-49-8205A>C MANE Select	ENSP00000334474.5:n.-49-8205A>C
ENST00000334512.9:c.-49-8205A>C	ENSP00000334474.5:n.-49-8205A>C
NM_020338.3:c.-49-8205A>C	NP_065071.1:n.-49-8205A>C
XM_005269987.3:c.-49-8205A>C	XP_005270044.1:n.-49-8205A>C
XM_005269988.2:c.-49-8205A>C	XP_005270045.1:n.-49-8205A>C
XM_006717923.2:c.-49-8205A>C	XP_006717986.1:n.-49-8205A>C
XM_006717924.2:c.-49-8205A>C	XP_006717987.1:n.-49-8205A>C
XM_006717925.2:c.-49-8205A>C	XP_006717988.1:n.-49-8205A>C
XM_005269987.5:c.-49-8205A>C	XP_005270044.1:n.-49-8205A>C
XM_005269988.3:c.-49-8205A>C	XP_005270045.1:n.-49-8205A>C
XM_006717923.3:c.-49-8205A>C	XP_006717986.1:n.-49-8205A>C
XM_006717924.3:c.-49-8205A>C	XP_006717987.1:n.-49-8205A>C
XM_006717925.3:c.-49-8205A>C	XP_006717988.1:n.-49-8205A>C
NM_020338.4:c.-49-8205A>C MANE Select	NP_065071.1:n.-49-8205A>C