Canonical Allele Identifier: CA2404069438
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1939793776
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36862337del , CM000684.2:g.36862337del GRCh38
NC_000022.10:g.37258379del , CM000684.1:g.37258379del GRCh37
NC_000022.9:g.35588325del NCBI36
NG_023400.1:g.6350del , LRG_159:g.6350del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248899.11:c.32+1134del (NCF4) MANE Select ENSP00000248899.6:n.32+1134del
ENST00000397147.7:c.32+1134del (NCF4) ENSP00000380334.4:n.32+1134del
ENST00000650827.1:c.-328del (NCF4) ENSP00000498212.1:n.-328del
ENST00000248899.10:c.32+1134del (NCF4) ENSP00000248899.6:n.32+1134del
ENST00000397147.6:c.32+1134del (NCF4) ENSP00000380334.4:n.32+1134del
ENST00000447071.5:c.-193+1134del (NCF4) ENSP00000414958.1:n.-193+1134del
NM_000631.4:c.32+1134del (NCF4) NP_000622.2:n.32+1134del
NM_013416.3:c.32+1134del , LRG_159t1:c.32+1134del (NCF4) NP_038202.2:n.32+1134del
XM_011530198.1:c.-318del (NCF4) XP_011528500.1:n.-318del
XM_011530199.1:c.97+522del (NCF4) XP_011528501.1:n.97+522del
NR_147197.1:n.351+7756del (NCF4-AS1)
XM_017028808.1:c.-278+522del (NCF4) XP_016884297.1:n.-278+522del
NM_000631.5:c.32+1134del (NCF4) MANE Select NP_000622.2:n.32+1134del
NM_013416.4:c.32+1134del (NCF4) NP_038202.2:n.32+1134del
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