Canonical Allele Identifier: CA514363356

Gene: NCF4 NCF4-AS1

Linked Data

• COSMIC: COSM5393543 ; COSM5393544
• MyVariant Identifiers: chr22:g.37261029C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864987C>T , CM000684.2:g.36864987C>T	GRCh38
NC_000022.10:g.37261029C>T , CM000684.1:g.37261029C>T	GRCh37
NC_000022.9:g.35590975C>T	NCBI36
NG_023400.1:g.9000C>T , LRG_159:g.9000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.186C>T (NCF4) MANE Select	ENSP00000248899.6:p.Phe62=
ENST00000397147.7:c.186C>T (NCF4)	ENSP00000380334.4:p.Phe62=
ENST00000650698.1:c.-124C>T (NCF4)	ENSP00000498381.1:n.-124C>T
ENST00000650827.1:c.-124C>T (NCF4)	ENSP00000498212.1:n.-124C>T
ENST00000651053.1:n.491C>T (NCF4)
ENST00000248899.10:c.186C>T (NCF4)	ENSP00000248899.6:p.Phe62=
ENST00000397147.6:c.186C>T (NCF4)	ENSP00000380334.4:p.Phe62=
ENST00000447071.5:c.-124C>T (NCF4)	ENSP00000414958.1:n.-124C>T
NM_000631.4:c.186C>T (NCF4)	NP_000622.2:p.Phe62=
NM_013416.3:c.186C>T , LRG_159t1:c.186C>T (NCF4)	NP_038202.2:p.Phe62=
XM_011530198.1:c.360C>T (NCF4)	XP_011528500.1:p.Phe120=
XM_011530199.1:c.330C>T (NCF4)	XP_011528501.1:p.Phe110=
NR_147197.1:n.351+5106G>A (NCF4-AS1)
XM_017028808.1:c.-124C>T (NCF4)	XP_016884297.1:n.-124C>T
NM_000631.5:c.186C>T (NCF4) MANE Select	NP_000622.2:p.Phe62=
NM_013416.4:c.186C>T (NCF4)	NP_038202.2:p.Phe62=