Canonical Allele Identifier: CA2229856784

Gene: ZFP90

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68566364T= , CM000678.2:g.68566364T=	GRCh38
NC_000016.9:g.68600267T= , CM000678.1:g.68600267T=	GRCh37
NC_000016.8:g.67157768T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000563169.7:c.*1666T= MANE Select	ENSP00000454418.2:n.*1666T=
ENST00000398253.6:c.*1666T=	ENSP00000381304.2:n.*1666T=
ENST00000564558.5:c.*3492T=	ENSP00000457129.1:n.*3492T=
ENST00000570495.5:c.*1666T=	ENSP00000460547.1:n.*1666T=
ENST00000573113.3:c.223+7796T=	ENSP00000458410.2:n.223+7796T=
ENST00000611381.4:c.256+7796T=	ENSP00000480309.1:n.256+7796T=
NM_001305203.1:c.*1666T=	NP_001292132.1:n.*1666T=
NM_001305204.1:c.256+7796T=	NP_001292133.1:n.256+7796T=
NM_001305206.1:c.*3350T=	NP_001292135.1:n.*3350T=
NM_001305207.1:c.*3350T=	NP_001292136.1:n.*3350T=
NM_001305208.1:c.*3350T=	NP_001292137.1:n.*3350T=
NM_133458.2:c.*1666T=	NP_597715.2:n.*1666T=
NM_133458.3:c.*1666T=	NP_597715.2:n.*1666T=
NR_130976.1:n.3977T=
NR_130977.1:n.3927T=
NR_130978.1:n.3985T=
XM_005255804.2:c.*1666T=	XP_005255861.1:n.*1666T=
XM_011522873.1:c.256+7796T=	XP_011521175.1:n.256+7796T=
XM_017022952.2:c.*1666T=	XP_016878441.1:n.*1666T=
XM_024450159.1:c.*1666T=	XP_024305927.1:n.*1666T=
NM_001305203.2:c.*1666T= MANE Select	NP_001292132.1:n.*1666T=
NM_001305206.2:c.*3350T=	NP_001292135.1:n.*3350T=
NM_001305207.2:c.*3350T=	NP_001292136.1:n.*3350T=
NM_001305208.2:c.*3350T=	NP_001292137.1:n.*3350T=
NM_133458.4:c.*1666T=	NP_597715.2:n.*1666T=
NR_130976.2:n.3899T=
NR_130977.2:n.3849T=
NR_130978.2:n.3907T=
NM_001305204.2:c.256+7796T=	NP_001292133.1:n.256+7796T=