Canonical Allele Identifier: CA377415720

Gene: ZMIZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79277309C>T , CM000672.2:g.79277309C>T	GRCh38
NC_000010.10:g.81037066C>T , CM000672.1:g.81037066C>T	GRCh37
NC_000010.9:g.80707072C>T	NCBI36
NG_028289.1:g.213275C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020338.4:c.409C>T MANE Select	NP_065071.1:p.Pro137Ser
ENST00000334512.10:c.409C>T MANE Select	ENSP00000334474.5:p.Pro137Ser
NM_020338.3:c.409C>T	NP_065071.1:p.Pro137Ser
ENST00000334512.9:c.409C>T	ENSP00000334474.5:p.Pro137Ser
ENST00000472035.5:n.199C>T
ENST00000478357.1:n.131C>T
ENST00000611351.1:c.409C>T	ENSP00000481736.1:p.Pro137Ser
XM_005269987.3:c.409C>T	XP_005270044.1:p.Pro137Ser
XM_005269987.5:c.409C>T	XP_005270044.1:p.Pro137Ser
XM_005269988.2:c.409C>T	XP_005270045.1:p.Pro137Ser
XM_005269988.3:c.409C>T	XP_005270045.1:p.Pro137Ser
XM_006717923.2:c.409C>T	XP_006717986.1:p.Pro137Ser
XM_006717923.3:c.409C>T	XP_006717986.1:p.Pro137Ser
XM_006717924.2:c.409C>T	XP_006717987.1:p.Pro137Ser
XM_006717924.3:c.409C>T	XP_006717987.1:p.Pro137Ser
XM_006717925.2:c.409C>T	XP_006717988.1:p.Pro137Ser
XM_006717925.3:c.409C>T	XP_006717988.1:p.Pro137Ser
XM_011539978.1:c.37C>T	XP_011538280.1:p.Pro13Ser
XM_011539978.2:c.37C>T	XP_011538280.1:p.Pro13Ser
XM_011539979.1:c.37C>T	XP_011538281.1:p.Pro13Ser
XM_011539980.1:c.37C>T	XP_011538282.1:p.Pro13Ser
XM_011539980.3:c.37C>T	XP_011538282.1:p.Pro13Ser
XM_017016440.2:c.256C>T	XP_016871929.1:p.Pro86Ser
XM_017016441.1:c.37C>T	XP_016871930.1:p.Pro13Ser
XM_017016442.1:c.37C>T	XP_016871931.1:p.Pro13Ser
XM_017016443.1:c.37C>T	XP_016871932.1:p.Pro13Ser