Canonical Allele Identifier: CA6014603
Gene: ZFP91 HGNC NCBI
ZFP91-CNTF HGNC NCBI
COSMIC:
COSM3752520 (not active)
COSM3752521 (not active)
MyVariant.info:
GRCh38 chr11:g.58610951A>G
GRCh37 chr11:g.58378424A>G
Revel Score:
ENST00000316059 (MANE Select) 0.100
ENST00000389918 0.100
gnomAD v2:
11:58378424 A / G
gnomAD v3:
11:58610951 A / G
gnomAD v4:
chr11-58610951-A-G
Joint Max Group AF 0.28909379 (MID)
Genomes Max Group AF 0.26318605 (SAS)
Exomes Max Group AF 0.28587383 (MID)
dbSNP:
8373
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.58610951A>G , CM000673.2:g.58610951A>G GRCh38
NC_000011.9:g.58378424A>G , CM000673.1:g.58378424A>G GRCh37
NC_000011.8:g.58135000A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316059.7:c.619A>G (ZFP91) MANE Select ENSP00000339030.5:p.Ser207Gly
ENST00000316059.6:c.619A>G (ZFP91) ENSP00000339030.5:p.Ser207Gly
ENST00000389919.8:c.619A>G (ZFP91-CNTF) ENSP00000455911.1:p.Ser207Gly
ENST00000422974.2:c.100A>G (ZFP91-CNTF) ENSP00000457288.1:p.Ser34Gly
NM_001197051.1:c.618-2A>G (ZFP91) NP_001183980.1:n.618-2A>G
NM_053023.4:c.619A>G (ZFP91) NP_444251.1:p.Ser207Gly
NR_024091.1:n.787A>G (ZFP91-CNTF)
NM_053023.5:c.619A>G (ZFP91) MANE Select NP_444251.1:p.Ser207Gly
NM_001197051.2:c.618-2A>G (ZFP91) NP_001183980.1:n.618-2A>G
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