Canonical Allele Identifier: CA377337352

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79298479C>G , CM000672.2:g.79298479C>G	GRCh38
NC_000010.10:g.81058236C>G , CM000672.1:g.81058236C>G	GRCh37
NC_000010.9:g.80728242C>G	NCBI36
NG_028289.1:g.234445C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.1565C>G MANE Select	ENSP00000334474.5:p.Pro522Arg
ENST00000334512.9:c.1565C>G	ENSP00000334474.5:p.Pro522Arg
ENST00000446377.3:c.1286C>G	ENSP00000401558.3:p.Pro429Arg
ENST00000611351.1:c.458+8672C>G	ENSP00000481736.1:n.458+8672C>G
NM_020338.3:c.1565C>G	NP_065071.1:p.Pro522Arg
XM_005269987.3:c.1583C>G	XP_005270044.1:p.Pro528Arg
XM_005269988.2:c.1583C>G	XP_005270045.1:p.Pro528Arg
XM_006717923.2:c.1583C>G	XP_006717986.1:p.Pro528Arg
XM_006717924.2:c.1583C>G	XP_006717987.1:p.Pro528Arg
XM_006717925.2:c.1583C>G	XP_006717988.1:p.Pro528Arg
XM_011539978.1:c.1211C>G	XP_011538280.1:p.Pro404Arg
XM_011539979.1:c.1211C>G	XP_011538281.1:p.Pro404Arg
XM_011539980.1:c.1193C>G	XP_011538282.1:p.Pro398Arg
XM_005269987.5:c.1583C>G	XP_005270044.1:p.Pro528Arg
XM_005269988.3:c.1583C>G	XP_005270045.1:p.Pro528Arg
XM_006717923.3:c.1583C>G	XP_006717986.1:p.Pro528Arg
XM_006717924.3:c.1583C>G	XP_006717987.1:p.Pro528Arg
XM_006717925.3:c.1583C>G	XP_006717988.1:p.Pro528Arg
XM_011539978.2:c.1211C>G	XP_011538280.1:p.Pro404Arg
XM_011539980.3:c.1193C>G	XP_011538282.1:p.Pro398Arg
XM_017016440.2:c.1430C>G	XP_016871929.1:p.Pro477Arg
XM_017016441.1:c.1211C>G	XP_016871930.1:p.Pro404Arg
XM_017016442.1:c.1193C>G	XP_016871931.1:p.Pro398Arg
XM_017016443.1:c.1211C>G	XP_016871932.1:p.Pro404Arg
NM_020338.4:c.1565C>G MANE Select	NP_065071.1:p.Pro522Arg