Canonical Allele Identifier: CA752888146

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs369648488
• MyVariant Identifiers: chr22:g.37260869_37260877del (hg19) ; chr22:g.36864827_36864835del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864836_36864844del , CM000684.2:g.36864836_36864844del	GRCh38
NC_000022.10:g.37260878_37260886del , CM000684.1:g.37260878_37260886del	GRCh37
NC_000022.9:g.35590824_35590832del	NCBI36
NG_023400.1:g.8849_8857del , LRG_159:g.8849_8857del

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.118-83_118-75del (NCF4) MANE Select	ENSP00000248899.6:n.118-83_118-75del
ENST00000397147.7:c.118-83_118-75del (NCF4)	ENSP00000380334.4:n.118-83_118-75del
ENST00000650698.1:c.-192-83_-192-75del (NCF4)	ENSP00000498381.1:n.-192-83_-192-75del
ENST00000650827.1:c.-192-83_-192-75del (NCF4)	ENSP00000498212.1:n.-192-83_-192-75del
ENST00000651053.1:n.423-83_423-75del (NCF4)
ENST00000248899.10:c.118-83_118-75del (NCF4)	ENSP00000248899.6:n.118-83_118-75del
ENST00000397147.6:c.118-83_118-75del (NCF4)	ENSP00000380334.4:n.118-83_118-75del
ENST00000447071.5:c.-192-83_-192-75del (NCF4)	ENSP00000414958.1:n.-192-83_-192-75del
NM_000631.4:c.118-83_118-75del (NCF4)	NP_000622.2:n.118-83_118-75del
NM_013416.3:c.118-83_118-75del , LRG_159t1:c.118-83_118-75del (NCF4)	NP_038202.2:n.118-83_118-75del
XM_011530198.1:c.292-83_292-75del (NCF4)	XP_011528500.1:n.292-83_292-75del
XM_011530199.1:c.262-83_262-75del (NCF4)	XP_011528501.1:n.262-83_262-75del
NR_147197.1:n.351+5258_351+5266del (NCF4-AS1)
XM_017028808.1:c.-192-83_-192-75del (NCF4)	XP_016884297.1:n.-192-83_-192-75del
NM_000631.5:c.118-83_118-75del (NCF4) MANE Select	NP_000622.2:n.118-83_118-75del
NM_013416.4:c.118-83_118-75del (NCF4)	NP_038202.2:n.118-83_118-75del