Canonical Allele Identifier: CA2776494892

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789296T>C , CM000669.2:g.74789296T>C	GRCh38
NC_000007.13:g.74203640T>C , CM000669.1:g.74203640T>C	GRCh37
NC_000007.12:g.73841576T>C	NCBI36
NG_009078.2:g.20333T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*136T>C MANE Select	ENSP00000289473.4:n.*136T>C
ENST00000289473.10:c.*136T>C	ENSP00000289473.4:n.*136T>C
ENST00000289473.8:c.*136T>C	ENSP00000289473.4:n.*136T>C
ENST00000398421.6:n.2336T>C
ENST00000455062.2:n.1418T>C
NM_000265.5:c.*136T>C	NP_000256.4:n.*136T>C
XM_005250543.3:c.*230T>C	XP_005250600.2:n.*230T>C
XM_011516498.1:c.*183T>C	XP_011514800.1:n.*183T>C
XM_011516501.1:c.*136T>C	XP_011514803.1:n.*136T>C
NM_000265.6:c.*136T>C	NP_000256.4:n.*136T>C
NM_000265.7:c.*136T>C MANE Select	NP_000256.4:n.*136T>C