Canonical Allele Identifier: CA283292973

Gene: ZFP90

Linked Data

• dbSNP Id: rs771413384
• gnomAD v2: 16-68600282-G-C
• gnomAD v3: 16-68566379-G-C
• gnomAD v4: 16-68566379-G-C
• MyVariant Identifiers: chr16:g.68600282G>C (hg19) ; chr16:g.68566379G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68566379G>C , CM000678.2:g.68566379G>C	GRCh38
NC_000016.9:g.68600282G>C , CM000678.1:g.68600282G>C	GRCh37
NC_000016.8:g.67157783G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000563169.7:c.*1681G>C MANE Select	ENSP00000454418.2:n.*1681G>C
ENST00000398253.6:c.*1681G>C	ENSP00000381304.2:n.*1681G>C
ENST00000564558.5:c.*3507G>C	ENSP00000457129.1:n.*3507G>C
ENST00000570495.5:c.*1681G>C	ENSP00000460547.1:n.*1681G>C
ENST00000573113.3:c.223+7811G>C	ENSP00000458410.2:n.223+7811G>C
ENST00000611381.4:c.256+7811G>C	ENSP00000480309.1:n.256+7811G>C
NM_001305203.1:c.*1681G>C	NP_001292132.1:n.*1681G>C
NM_001305204.1:c.256+7811G>C	NP_001292133.1:n.256+7811G>C
NM_001305206.1:c.*3365G>C	NP_001292135.1:n.*3365G>C
NM_001305207.1:c.*3365G>C	NP_001292136.1:n.*3365G>C
NM_001305208.1:c.*3365G>C	NP_001292137.1:n.*3365G>C
NM_133458.2:c.*1681G>C	NP_597715.2:n.*1681G>C
NM_133458.3:c.*1681G>C	NP_597715.2:n.*1681G>C
NR_130976.1:n.3992G>C
NR_130977.1:n.3942G>C
NR_130978.1:n.4000G>C
XM_005255804.2:c.*1681G>C	XP_005255861.1:n.*1681G>C
XM_011522873.1:c.256+7811G>C	XP_011521175.1:n.256+7811G>C
XM_017022952.2:c.*1681G>C	XP_016878441.1:n.*1681G>C
XM_024450159.1:c.*1681G>C	XP_024305927.1:n.*1681G>C
NM_001305203.2:c.*1681G>C MANE Select	NP_001292132.1:n.*1681G>C
NM_001305206.2:c.*3365G>C	NP_001292135.1:n.*3365G>C
NM_001305207.2:c.*3365G>C	NP_001292136.1:n.*3365G>C
NM_001305208.2:c.*3365G>C	NP_001292137.1:n.*3365G>C
NM_133458.4:c.*1681G>C	NP_597715.2:n.*1681G>C
NR_130976.2:n.3914G>C
NR_130977.2:n.3864G>C
NR_130978.2:n.3922G>C
NM_001305204.2:c.256+7811G>C	NP_001292133.1:n.256+7811G>C