Canonical Allele Identifier: CA411379384

Gene: NCF4 NCF4-AS1

Linked Data

• MyVariant Identifiers: chr22:g.37261084G>T (hg19) ; chr22:g.36865042G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36865042G>T , CM000684.2:g.36865042G>T	GRCh38
NC_000022.10:g.37261084G>T , CM000684.1:g.37261084G>T	GRCh37
NC_000022.9:g.35591030G>T	NCBI36
NG_023400.1:g.9055G>T , LRG_159:g.9055G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.241G>T (NCF4) MANE Select	ENSP00000248899.6:p.Ala81Ser
ENST00000397147.7:c.241G>T (NCF4)	ENSP00000380334.4:p.Ala81Ser
ENST00000650698.1:c.-69G>T (NCF4)	ENSP00000498381.1:n.-69G>T
ENST00000650827.1:c.-69G>T (NCF4)	ENSP00000498212.1:n.-69G>T
ENST00000651053.1:n.546G>T (NCF4)
ENST00000248899.10:c.241G>T (NCF4)	ENSP00000248899.6:p.Ala81Ser
ENST00000397147.6:c.241G>T (NCF4)	ENSP00000380334.4:p.Ala81Ser
ENST00000447071.5:c.-69G>T (NCF4)	ENSP00000414958.1:n.-69G>T
NM_000631.4:c.241G>T (NCF4)	NP_000622.2:p.Ala81Ser
NM_013416.3:c.241G>T , LRG_159t1:c.241G>T (NCF4)	NP_038202.2:p.Ala81Ser
XM_011530198.1:c.415G>T (NCF4)	XP_011528500.1:p.Ala139Ser
XM_011530199.1:c.385G>T (NCF4)	XP_011528501.1:p.Ala129Ser
NR_147197.1:n.351+5051C>A (NCF4-AS1)
XM_017028808.1:c.-69G>T (NCF4)	XP_016884297.1:n.-69G>T
NM_000631.5:c.241G>T (NCF4) MANE Select	NP_000622.2:p.Ala81Ser
NM_013416.4:c.241G>T (NCF4)	NP_038202.2:p.Ala81Ser