Canonical Allele Identifier: CA1922019910
Gene: ZMIZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79085652_79085654delinsACG , CM000672.2:g.79085652_79085654delinsACG GRCh38
NC_000010.10:g.80845409_80845411delinsACG , CM000672.1:g.80845409_80845411delinsACG GRCh37
NC_000010.9:g.80515415_80515417delinsACG NCBI36
NG_028289.1:g.21618_21620delinsACG

Transcript Alleles

HGVS Amino-acid change
ENST00000334512.10:c.-337+16382_-337+16384delinsACG MANE Select ENSP00000334474.5:n.-337+16382_-337+16384delinsACG
ENST00000334512.9:c.-337+16382_-337+16384delinsACG ENSP00000334474.5:n.-337+16382_-337+16384delinsACG
NM_020338.3:c.-337+16382_-337+16384delinsACG NP_065071.1:n.-337+16382_-337+16384delinsACG
XM_005269988.2:c.-337+16382_-337+16384delinsACG XP_005270045.1:n.-337+16382_-337+16384delinsACG
XM_006717923.2:c.-334+16382_-334+16384delinsACG XP_006717986.1:n.-334+16382_-334+16384delinsACG
XM_006717924.2:c.-256+16382_-256+16384delinsACG XP_006717987.1:n.-256+16382_-256+16384delinsACG
XM_006717925.2:c.-337+16382_-337+16384delinsACG XP_006717988.1:n.-337+16382_-337+16384delinsACG
XM_005269988.3:c.-337+16382_-337+16384delinsACG XP_005270045.1:n.-337+16382_-337+16384delinsACG
XM_006717923.3:c.-334+16382_-334+16384delinsACG XP_006717986.1:n.-334+16382_-334+16384delinsACG
XM_006717924.3:c.-256+16382_-256+16384delinsACG XP_006717987.1:n.-256+16382_-256+16384delinsACG
XM_006717925.3:c.-337+16382_-337+16384delinsACG XP_006717988.1:n.-337+16382_-337+16384delinsACG
NM_020338.4:c.-337+16382_-337+16384delinsACG MANE Select NP_065071.1:n.-337+16382_-337+16384delinsACG