Canonical Allele Identifier: CA455897679

Gene: NCF1

Linked Data

• MyVariant Identifiers: chr7:g.74203423G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789079G>T , CM000669.2:g.74789079G>T	GRCh38
NC_000007.13:g.74203423G>T , CM000669.1:g.74203423G>T	GRCh37
NC_000007.12:g.73841359G>T	NCBI36
NG_009078.2:g.20116G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1092G>T MANE Select	ENSP00000289473.4:p.Ala364=
ENST00000289473.10:c.1092G>T	ENSP00000289473.4:p.Ala364=
ENST00000289473.8:c.1092G>T	ENSP00000289473.4:p.Ala364=
ENST00000398421.6:n.2119G>T
ENST00000455062.2:n.1201G>T
NM_000265.5:c.1092G>T	NP_000256.4:p.Ala364=
XM_005250543.3:c.*13G>T	XP_005250600.2:n.*13G>T
XM_011516498.1:c.1091G>T	XP_011514800.1:p.Arg364Leu
XM_011516501.1:c.699G>T	XP_011514803.1:p.Ala233=
NM_000265.6:c.1092G>T	NP_000256.4:p.Ala364=
NM_000265.7:c.1092G>T MANE Select	NP_000256.4:p.Ala364=