Canonical Allele Identifier: CA1025510088

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1939883880
• gnomAD v3: 22-36864818-T-TCATGATCTTCCTCCTCCTCCTCCTCCC
• gnomAD v4: 22-36864818-T-TCATGATCTTCCTCCTCCTCCTCCTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864821_36864822insGATCTTCCTCCTCCTCCTCCTCCCCAT , CM000684.2:g.36864821_36864822insGATCTTCCTCCTCCTCCTCCTCCCCAT	GRCh38
NC_000022.10:g.37260863_37260864insGATCTTCCTCCTCCTCCTCCTCCCCAT , CM000684.1:g.37260863_37260864insGATCTTCCTCCTCCTCCTCCTCCCCAT	GRCh37
NC_000022.9:g.35590809_35590810insGATCTTCCTCCTCCTCCTCCTCCCCAT	NCBI36
NG_023400.1:g.8834_8835insGATCTTCCTCCTCCTCCTCCTCCCCAT , LRG_159:g.8834_8835insGATCTTCCTCCTCCTCCTCCTCCCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4) MANE Select	ENSP00000248899.6:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCC...
ENST00000397147.7:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000380334.4:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCC...
ENST00000650698.1:c.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000498381.1:n.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCC...
ENST00000650827.1:c.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000498212.1:n.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCC...
ENST00000651053.1:n.423-98_423-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)
ENST00000248899.10:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000248899.6:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCC...
ENST00000397147.6:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000380334.4:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCC...
ENST00000447071.5:c.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	ENSP00000414958.1:n.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCC...
NM_000631.4:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	NP_000622.2:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT
NM_013416.3:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT , LRG_159t1:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	NP_038202.2:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT
XM_011530198.1:c.292-98_292-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	XP_011528500.1:n.292-98_292-97insGATCTTCCTCCTCCTCCTCCTCCCCAT
XM_011530199.1:c.262-98_262-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	XP_011528501.1:n.262-98_262-97insGATCTTCCTCCTCCTCCTCCTCCCCAT
NR_147197.1:n.351+5274_351+5275insGGGAGGAGGAGGAGGAGGAAGATCATG (NCF4-AS1)
XM_017028808.1:c.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	XP_016884297.1:n.-192-98_-192-97insGATCTTCCTCCTCCTCCTCCTCCCCA...
NM_000631.5:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4) MANE Select	NP_000622.2:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT
NM_013416.4:c.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT (NCF4)	NP_038202.2:n.118-98_118-97insGATCTTCCTCCTCCTCCTCCTCCCCAT