Canonical Allele Identifier: CA411378933
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36864956A>T , CM000684.2:g.36864956A>T GRCh38
NC_000022.10:g.37260998A>T , CM000684.1:g.37260998A>T GRCh37
NC_000022.9:g.35590944A>T NCBI36
NG_023400.1:g.8969A>T , LRG_159:g.8969A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248899.11:c.155A>T (NCF4) MANE Select ENSP00000248899.6:p.Lys52Met
ENST00000397147.7:c.155A>T (NCF4) ENSP00000380334.4:p.Lys52Met
ENST00000650698.1:c.-155A>T (NCF4) ENSP00000498381.1:n.-155A>T
ENST00000650827.1:c.-155A>T (NCF4) ENSP00000498212.1:n.-155A>T
ENST00000651053.1:n.460A>T (NCF4)
ENST00000248899.10:c.155A>T (NCF4) ENSP00000248899.6:p.Lys52Met
ENST00000397147.6:c.155A>T (NCF4) ENSP00000380334.4:p.Lys52Met
ENST00000447071.5:c.-155A>T (NCF4) ENSP00000414958.1:n.-155A>T
NM_000631.4:c.155A>T (NCF4) NP_000622.2:p.Lys52Met
NM_013416.3:c.155A>T , LRG_159t1:c.155A>T (NCF4) NP_038202.2:p.Lys52Met
XM_011530198.1:c.329A>T (NCF4) XP_011528500.1:p.Lys110Met
XM_011530199.1:c.299A>T (NCF4) XP_011528501.1:p.Lys100Met
NR_147197.1:n.351+5137T>A (NCF4-AS1)
XM_017028808.1:c.-155A>T (NCF4) XP_016884297.1:n.-155A>T
NM_000631.5:c.155A>T (NCF4) MANE Select NP_000622.2:p.Lys52Met
NM_013416.4:c.155A>T (NCF4) NP_038202.2:p.Lys52Met