Canonical Allele Identifier: CA2818898648

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862397G>T , CM000684.2:g.36862397G>T	GRCh38
NC_000022.10:g.37258439G>T , CM000684.1:g.37258439G>T	GRCh37
NC_000022.9:g.35588385G>T	NCBI36
NG_023400.1:g.6410G>T , LRG_159:g.6410G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.32+1194G>T (NCF4) MANE Select	ENSP00000248899.6:n.32+1194G>T
ENST00000397147.7:c.32+1194G>T (NCF4)	ENSP00000380334.4:n.32+1194G>T
ENST00000650827.1:c.-278+10G>T (NCF4)	ENSP00000498212.1:n.-278+10G>T
ENST00000248899.10:c.32+1194G>T (NCF4)	ENSP00000248899.6:n.32+1194G>T
ENST00000397147.6:c.32+1194G>T (NCF4)	ENSP00000380334.4:n.32+1194G>T
ENST00000447071.5:c.-193+1194G>T (NCF4)	ENSP00000414958.1:n.-193+1194G>T
NM_000631.4:c.32+1194G>T (NCF4)	NP_000622.2:n.32+1194G>T
NM_013416.3:c.32+1194G>T , LRG_159t1:c.32+1194G>T (NCF4)	NP_038202.2:n.32+1194G>T
XM_011530198.1:c.-258G>T (NCF4)	XP_011528500.1:n.-258G>T
XM_011530199.1:c.97+582G>T (NCF4)	XP_011528501.1:n.97+582G>T
NR_147197.1:n.351+7696C>A (NCF4-AS1)
XM_017028808.1:c.-278+582G>T (NCF4)	XP_016884297.1:n.-278+582G>T
NM_000631.5:c.32+1194G>T (NCF4) MANE Select	NP_000622.2:n.32+1194G>T
NM_013416.4:c.32+1194G>T (NCF4)	NP_038202.2:n.32+1194G>T