Canonical Allele Identifier: CA594668499

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs1564641543
• gnomAD v2: 10-80845410-CG-C
• gnomAD v3: 10-79085653-CG-C
• gnomAD v4: 10-79085653-CG-C
• MyVariant Identifiers: chr10:g.80845411del (hg19) ; chr10:g.79085654del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79085654del , CM000672.2:g.79085654del	GRCh38
NC_000010.10:g.80845411del , CM000672.1:g.80845411del	GRCh37
NC_000010.9:g.80515417del	NCBI36
NG_028289.1:g.21620del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.-337+16384del MANE Select	ENSP00000334474.5:n.-337+16384del
ENST00000334512.9:c.-337+16384del	ENSP00000334474.5:n.-337+16384del
NM_020338.3:c.-337+16384del	NP_065071.1:n.-337+16384del
XM_005269988.2:c.-337+16384del	XP_005270045.1:n.-337+16384del
XM_006717923.2:c.-334+16384del	XP_006717986.1:n.-334+16384del
XM_006717924.2:c.-256+16384del	XP_006717987.1:n.-256+16384del
XM_006717925.2:c.-337+16384del	XP_006717988.1:n.-337+16384del
XM_005269988.3:c.-337+16384del	XP_005270045.1:n.-337+16384del
XM_006717923.3:c.-334+16384del	XP_006717986.1:n.-334+16384del
XM_006717924.3:c.-256+16384del	XP_006717987.1:n.-256+16384del
XM_006717925.3:c.-337+16384del	XP_006717988.1:n.-337+16384del
NM_020338.4:c.-337+16384del MANE Select	NP_065071.1:n.-337+16384del