Canonical Allele Identifier: CA2547375384
Gene: ZMIZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79256203C>T , CM000672.2:g.79256203C>T GRCh38
NC_000010.10:g.81015960C>T , CM000672.1:g.81015960C>T GRCh37
NC_000010.9:g.80685966C>T NCBI36
NG_028289.1:g.192169C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000334512.10:c.281-20978C>T MANE Select ENSP00000334474.5:n.281-20978C>T
ENST00000334512.9:c.281-20978C>T ENSP00000334474.5:n.281-20978C>T
ENST00000472035.5:n.70+12465C>T
ENST00000611351.1:c.281-20978C>T ENSP00000481736.1:n.281-20978C>T
NM_020338.3:c.281-20978C>T NP_065071.1:n.281-20978C>T
XM_005269987.3:c.281-20978C>T XP_005270044.1:n.281-20978C>T
XM_005269988.2:c.281-20978C>T XP_005270045.1:n.281-20978C>T
XM_006717923.2:c.281-20978C>T XP_006717986.1:n.281-20978C>T
XM_006717924.2:c.281-20978C>T XP_006717987.1:n.281-20978C>T
XM_006717925.2:c.281-20978C>T XP_006717988.1:n.281-20978C>T
XM_011539978.1:c.-93+12465C>T XP_011538280.1:n.-93+12465C>T
XM_011539979.1:c.-93+13234C>T XP_011538281.1:n.-93+13234C>T
XM_011539980.1:c.-93+12465C>T XP_011538282.1:n.-93+12465C>T
XM_005269987.5:c.281-20978C>T XP_005270044.1:n.281-20978C>T
XM_005269988.3:c.281-20978C>T XP_005270045.1:n.281-20978C>T
XM_006717923.3:c.281-20978C>T XP_006717986.1:n.281-20978C>T
XM_006717924.3:c.281-20978C>T XP_006717987.1:n.281-20978C>T
XM_006717925.3:c.281-20978C>T XP_006717988.1:n.281-20978C>T
XM_011539978.2:c.-93+12465C>T XP_011538280.1:n.-93+12465C>T
XM_011539980.3:c.-93+12465C>T XP_011538282.1:n.-93+12465C>T
XM_017016441.1:c.-93+13133C>T XP_016871930.1:n.-93+13133C>T
XM_017016442.1:c.-93+13234C>T XP_016871931.1:n.-93+13234C>T
XM_017016443.1:c.-93+13309C>T XP_016871932.1:n.-93+13309C>T
NM_020338.4:c.281-20978C>T MANE Select NP_065071.1:n.281-20978C>T