Canonical Allele Identifier: CA367956027

Gene: NCF1

Linked Data

• MyVariant Identifiers: chr7:g.74203443C>T (hg19) ; chr7:g.74789099C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789099C>T , CM000669.2:g.74789099C>T	GRCh38
NC_000007.13:g.74203443C>T , CM000669.1:g.74203443C>T	GRCh37
NC_000007.12:g.73841379C>T	NCBI36
NG_009078.2:g.20136C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1112C>T MANE Select	ENSP00000289473.4:p.Ala371Val
ENST00000289473.10:c.1112C>T	ENSP00000289473.4:p.Ala371Val
ENST00000289473.8:c.1112C>T	ENSP00000289473.4:p.Ala371Val
ENST00000398421.6:n.2139C>T
ENST00000455062.2:n.1221C>T
NM_000265.5:c.1112C>T	NP_000256.4:p.Ala371Val
XM_005250543.3:c.*33C>T	XP_005250600.2:n.*33C>T
XM_011516498.1:c.1111C>T	XP_011514800.1:p.Pro371Ser
XM_011516501.1:c.719C>T	XP_011514803.1:p.Ala240Val
NM_000265.6:c.1112C>T	NP_000256.4:p.Ala371Val
NM_000265.7:c.1112C>T MANE Select	NP_000256.4:p.Ala371Val