Canonical Allele Identifier: CA2788670887
Gene: ZMIZ1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79085678G>A , CM000672.2:g.79085678G>A GRCh38
NC_000010.10:g.80845435G>A , CM000672.1:g.80845435G>A GRCh37
NC_000010.9:g.80515441G>A NCBI36
NG_028289.1:g.21644G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334512.10:c.-337+16408G>A MANE Select ENSP00000334474.5:n.-337+16408G>A
ENST00000334512.9:c.-337+16408G>A ENSP00000334474.5:n.-337+16408G>A
NM_020338.3:c.-337+16408G>A NP_065071.1:n.-337+16408G>A
XM_005269988.2:c.-337+16408G>A XP_005270045.1:n.-337+16408G>A
XM_006717923.2:c.-334+16408G>A XP_006717986.1:n.-334+16408G>A
XM_006717924.2:c.-256+16408G>A XP_006717987.1:n.-256+16408G>A
XM_006717925.2:c.-337+16408G>A XP_006717988.1:n.-337+16408G>A
XM_005269988.3:c.-337+16408G>A XP_005270045.1:n.-337+16408G>A
XM_006717923.3:c.-334+16408G>A XP_006717986.1:n.-334+16408G>A
XM_006717924.3:c.-256+16408G>A XP_006717987.1:n.-256+16408G>A
XM_006717925.3:c.-337+16408G>A XP_006717988.1:n.-337+16408G>A
NM_020338.4:c.-337+16408G>A MANE Select NP_065071.1:n.-337+16408G>A
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