Canonical Allele Identifier: CA2229856925

Gene: ZFP90

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68566449C= , CM000678.2:g.68566449C=	GRCh38
NC_000016.9:g.68600352C= , CM000678.1:g.68600352C=	GRCh37
NC_000016.8:g.67157853C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000563169.7:c.*1751C= MANE Select	ENSP00000454418.2:n.*1751C=
ENST00000398253.6:c.*1751C=	ENSP00000381304.2:n.*1751C=
ENST00000564558.5:c.*3577C=	ENSP00000457129.1:n.*3577C=
ENST00000570495.5:c.*1751C=	ENSP00000460547.1:n.*1751C=
ENST00000573113.3:c.223+7881C=	ENSP00000458410.2:n.223+7881C=
ENST00000611381.4:c.256+7881C=	ENSP00000480309.1:n.256+7881C=
NM_001305203.1:c.*1751C=	NP_001292132.1:n.*1751C=
NM_001305204.1:c.256+7881C=	NP_001292133.1:n.256+7881C=
NM_001305206.1:c.*3435C=	NP_001292135.1:n.*3435C=
NM_001305207.1:c.*3435C=	NP_001292136.1:n.*3435C=
NM_001305208.1:c.*3435C=	NP_001292137.1:n.*3435C=
NM_133458.2:c.*1751C=	NP_597715.2:n.*1751C=
NM_133458.3:c.*1751C=	NP_597715.2:n.*1751C=
NR_130976.1:n.4062C=
NR_130977.1:n.4012C=
NR_130978.1:n.4070C=
XM_005255804.2:c.*1751C=	XP_005255861.1:n.*1751C=
XM_011522873.1:c.256+7881C=	XP_011521175.1:n.256+7881C=
XM_017022952.2:c.*1751C=	XP_016878441.1:n.*1751C=
XM_024450159.1:c.*1751C=	XP_024305927.1:n.*1751C=
NM_001305203.2:c.*1751C= MANE Select	NP_001292132.1:n.*1751C=
NM_001305206.2:c.*3435C=	NP_001292135.1:n.*3435C=
NM_001305207.2:c.*3435C=	NP_001292136.1:n.*3435C=
NM_001305208.2:c.*3435C=	NP_001292137.1:n.*3435C=
NM_133458.4:c.*1751C=	NP_597715.2:n.*1751C=
NR_130976.2:n.3984C=
NR_130977.2:n.3934C=
NR_130978.2:n.3992C=
NM_001305204.2:c.256+7881C=	NP_001292133.1:n.256+7881C=