Canonical Allele Identifier: CA411378903

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1939888127
• MyVariant Identifiers: chr22:g.37260994T>C (hg19) ; chr22:g.36864952T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864952T>C , CM000684.2:g.36864952T>C	GRCh38
NC_000022.10:g.37260994T>C , CM000684.1:g.37260994T>C	GRCh37
NC_000022.9:g.35590940T>C	NCBI36
NG_023400.1:g.8965T>C , LRG_159:g.8965T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.151T>C (NCF4) MANE Select	ENSP00000248899.6:p.Ser51Pro
ENST00000397147.7:c.151T>C (NCF4)	ENSP00000380334.4:p.Ser51Pro
ENST00000650698.1:c.-159T>C (NCF4)	ENSP00000498381.1:n.-159T>C
ENST00000650827.1:c.-159T>C (NCF4)	ENSP00000498212.1:n.-159T>C
ENST00000651053.1:n.456T>C (NCF4)
ENST00000248899.10:c.151T>C (NCF4)	ENSP00000248899.6:p.Ser51Pro
ENST00000397147.6:c.151T>C (NCF4)	ENSP00000380334.4:p.Ser51Pro
ENST00000447071.5:c.-159T>C (NCF4)	ENSP00000414958.1:n.-159T>C
NM_000631.4:c.151T>C (NCF4)	NP_000622.2:p.Ser51Pro
NM_013416.3:c.151T>C , LRG_159t1:c.151T>C (NCF4)	NP_038202.2:p.Ser51Pro
XM_011530198.1:c.325T>C (NCF4)	XP_011528500.1:p.Ser109Pro
XM_011530199.1:c.295T>C (NCF4)	XP_011528501.1:p.Ser99Pro
NR_147197.1:n.351+5141A>G (NCF4-AS1)
XM_017028808.1:c.-159T>C (NCF4)	XP_016884297.1:n.-159T>C
NM_000631.5:c.151T>C (NCF4) MANE Select	NP_000622.2:p.Ser51Pro
NM_013416.4:c.151T>C (NCF4)	NP_038202.2:p.Ser51Pro