Canonical Allele Identifier: CA2776494880

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789212G>C , CM000669.2:g.74789212G>C	GRCh38
NC_000007.13:g.74203556G>C , CM000669.1:g.74203556G>C	GRCh37
NC_000007.12:g.73841492G>C	NCBI36
NG_009078.2:g.20249G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*52G>C MANE Select	ENSP00000289473.4:n.*52G>C
ENST00000289473.10:c.*52G>C	ENSP00000289473.4:n.*52G>C
ENST00000289473.8:c.*52G>C	ENSP00000289473.4:n.*52G>C
ENST00000398421.6:n.2252G>C
ENST00000455062.2:n.1334G>C
NM_000265.5:c.*52G>C	NP_000256.4:n.*52G>C
XM_005250543.3:c.*146G>C	XP_005250600.2:n.*146G>C
XM_011516498.1:c.*99G>C	XP_011514800.1:n.*99G>C
XM_011516501.1:c.*52G>C	XP_011514803.1:n.*52G>C
NM_000265.6:c.*52G>C	NP_000256.4:n.*52G>C
NM_000265.7:c.*52G>C MANE Select	NP_000256.4:n.*52G>C