Canonical Allele Identifier: CA1025510119
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1939885307
gnomAD v4: 22-36864859-CCT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36864862_36864863del , CM000684.2:g.36864862_36864863del GRCh38
NC_000022.10:g.37260904_37260905del , CM000684.1:g.37260904_37260905del GRCh37
NC_000022.9:g.35590850_35590851del NCBI36
NG_023400.1:g.8875_8876del , LRG_159:g.8875_8876del

Transcript Alleles

HGVS Amino-acid change
ENST00000248899.11:c.118-57_118-56del (NCF4) MANE Select ENSP00000248899.6:n.118-57_118-56del
ENST00000397147.7:c.118-57_118-56del (NCF4) ENSP00000380334.4:n.118-57_118-56del
ENST00000650698.1:c.-192-57_-192-56del (NCF4) ENSP00000498381.1:n.-192-57_-192-56del
ENST00000650827.1:c.-192-57_-192-56del (NCF4) ENSP00000498212.1:n.-192-57_-192-56del
ENST00000651053.1:n.423-57_423-56del (NCF4)
ENST00000248899.10:c.118-57_118-56del (NCF4) ENSP00000248899.6:n.118-57_118-56del
ENST00000397147.6:c.118-57_118-56del (NCF4) ENSP00000380334.4:n.118-57_118-56del
ENST00000447071.5:c.-192-57_-192-56del (NCF4) ENSP00000414958.1:n.-192-57_-192-56del
NM_000631.4:c.118-57_118-56del (NCF4) NP_000622.2:n.118-57_118-56del
NM_013416.3:c.118-57_118-56del , LRG_159t1:c.118-57_118-56del (NCF4) NP_038202.2:n.118-57_118-56del
XM_011530198.1:c.292-57_292-56del (NCF4) XP_011528500.1:n.292-57_292-56del
XM_011530199.1:c.262-57_262-56del (NCF4) XP_011528501.1:n.262-57_262-56del
NR_147197.1:n.351+5232_351+5233del (NCF4-AS1)
XM_017028808.1:c.-192-57_-192-56del (NCF4) XP_016884297.1:n.-192-57_-192-56del
NM_000631.5:c.118-57_118-56del (NCF4) MANE Select NP_000622.2:n.118-57_118-56del
NM_013416.4:c.118-57_118-56del (NCF4) NP_038202.2:n.118-57_118-56del
Search 100 bp 5'
Search 100 bp 3'