Canonical Allele Identifier: CA1922019916
Gene: ZMIZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1842788144

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79085657dup , CM000672.2:g.79085657dup GRCh38
NC_000010.10:g.80845414dup , CM000672.1:g.80845414dup GRCh37
NC_000010.9:g.80515420dup NCBI36
NG_028289.1:g.21623dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000334512.10:c.-337+16387dup MANE Select ENSP00000334474.5:n.-337+16387dup
ENST00000334512.9:c.-337+16387dup ENSP00000334474.5:n.-337+16387dup
NM_020338.3:c.-337+16387dup NP_065071.1:n.-337+16387dup
XM_005269988.2:c.-337+16387dup XP_005270045.1:n.-337+16387dup
XM_006717923.2:c.-334+16387dup XP_006717986.1:n.-334+16387dup
XM_006717924.2:c.-256+16387dup XP_006717987.1:n.-256+16387dup
XM_006717925.2:c.-337+16387dup XP_006717988.1:n.-337+16387dup
XM_005269988.3:c.-337+16387dup XP_005270045.1:n.-337+16387dup
XM_006717923.3:c.-334+16387dup XP_006717986.1:n.-334+16387dup
XM_006717924.3:c.-256+16387dup XP_006717987.1:n.-256+16387dup
XM_006717925.3:c.-337+16387dup XP_006717988.1:n.-337+16387dup
NM_020338.4:c.-337+16387dup MANE Select NP_065071.1:n.-337+16387dup