Canonical Allele Identifier: CA323982350

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs373593526
• MyVariant Identifiers: chr22:g.37258338A>C (hg19) ; chr22:g.36862296A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862296A>C , CM000684.2:g.36862296A>C	GRCh38
NC_000022.10:g.37258338A>C , CM000684.1:g.37258338A>C	GRCh37
NC_000022.9:g.35588284A>C	NCBI36
NG_023400.1:g.6309A>C , LRG_159:g.6309A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1093A>C (NCF4) MANE Select	ENSP00000248899.6:n.32+1093A>C
ENST00000397147.7:c.32+1093A>C (NCF4)	ENSP00000380334.4:n.32+1093A>C
ENST00000248899.10:c.32+1093A>C (NCF4)	ENSP00000248899.6:n.32+1093A>C
ENST00000397147.6:c.32+1093A>C (NCF4)	ENSP00000380334.4:n.32+1093A>C
ENST00000447071.5:c.-193+1093A>C (NCF4)	ENSP00000414958.1:n.-193+1093A>C
NM_000631.4:c.32+1093A>C (NCF4)	NP_000622.2:n.32+1093A>C
NM_013416.3:c.32+1093A>C , LRG_159t1:c.32+1093A>C (NCF4)	NP_038202.2:n.32+1093A>C
XM_011530198.1:c.-359A>C (NCF4)	XP_011528500.1:n.-359A>C
XM_011530199.1:c.97+481A>C (NCF4)	XP_011528501.1:n.97+481A>C
NR_147197.1:n.351+7797T>G (NCF4-AS1)
XM_017028808.1:c.-278+481A>C (NCF4)	XP_016884297.1:n.-278+481A>C
NM_000631.5:c.32+1093A>C (NCF4) MANE Select	NP_000622.2:n.32+1093A>C
NM_013416.4:c.32+1093A>C (NCF4)	NP_038202.2:n.32+1093A>C