Canonical Allele Identifier: CA1103162925

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789245A>C , CM000669.2:g.74789245A>C	GRCh38
NC_000007.13:g.74203589A>C , CM000669.1:g.74203589A>C	GRCh37
NC_000007.12:g.73841525A>C	NCBI36
NG_009078.2:g.20282A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*85A>C MANE Select	ENSP00000289473.4:n.*85A>C
ENST00000289473.10:c.*85A>C	ENSP00000289473.4:n.*85A>C
ENST00000289473.8:c.*85A>C	ENSP00000289473.4:n.*85A>C
ENST00000398421.6:n.2285A>C
ENST00000455062.2:n.1367A>C
NM_000265.5:c.*85A>C	NP_000256.4:n.*85A>C
XM_005250543.3:c.*179A>C	XP_005250600.2:n.*179A>C
XM_011516498.1:c.*132A>C	XP_011514800.1:n.*132A>C
XM_011516501.1:c.*85A>C	XP_011514803.1:n.*85A>C
NM_000265.6:c.*85A>C	NP_000256.4:n.*85A>C
NM_000265.7:c.*85A>C MANE Select	NP_000256.4:n.*85A>C