Canonical Allele Identifier: CA2503286568

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864712_36864713insCTTT , CM000684.2:g.36864712_36864713insCTTT	GRCh38
NC_000022.10:g.37260754_37260755insCTTT , CM000684.1:g.37260754_37260755insCTTT	GRCh37
NC_000022.9:g.35590700_35590701insCTTT	NCBI36
NG_023400.1:g.8725_8726insCTTT , LRG_159:g.8725_8726insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.118-207_118-206insCTTT (NCF4) MANE Select	ENSP00000248899.6:n.118-207_118-206insCTTT
ENST00000397147.7:c.118-207_118-206insCTTT (NCF4)	ENSP00000380334.4:n.118-207_118-206insCTTT
ENST00000650698.1:c.-192-207_-192-206insCTTT (NCF4)	ENSP00000498381.1:n.-192-207_-192-206insCTTT
ENST00000650827.1:c.-192-207_-192-206insCTTT (NCF4)	ENSP00000498212.1:n.-192-207_-192-206insCTTT
ENST00000651053.1:n.423-207_423-206insCTTT (NCF4)
ENST00000248899.10:c.118-207_118-206insCTTT (NCF4)	ENSP00000248899.6:n.118-207_118-206insCTTT
ENST00000397147.6:c.118-207_118-206insCTTT (NCF4)	ENSP00000380334.4:n.118-207_118-206insCTTT
ENST00000447071.5:c.-192-207_-192-206insCTTT (NCF4)	ENSP00000414958.1:n.-192-207_-192-206insCTTT
NM_000631.4:c.118-207_118-206insCTTT (NCF4)	NP_000622.2:n.118-207_118-206insCTTT
NM_013416.3:c.118-207_118-206insCTTT , LRG_159t1:c.118-207_118-206insCTTT (NCF4)	NP_038202.2:n.118-207_118-206insCTTT
XM_011530198.1:c.292-207_292-206insCTTT (NCF4)	XP_011528500.1:n.292-207_292-206insCTTT
XM_011530199.1:c.262-207_262-206insCTTT (NCF4)	XP_011528501.1:n.262-207_262-206insCTTT
NR_147197.1:n.351+5383_351+5384insGAAA (NCF4-AS1)
XM_017028808.1:c.-192-207_-192-206insCTTT (NCF4)	XP_016884297.1:n.-192-207_-192-206insCTTT
NM_000631.5:c.118-207_118-206insCTTT (NCF4) MANE Select	NP_000622.2:n.118-207_118-206insCTTT
NM_013416.4:c.118-207_118-206insCTTT (NCF4)	NP_038202.2:n.118-207_118-206insCTTT