Canonical Allele Identifier: CA1103162913

Gene: NCF1

Linked Data

• gnomAD v3: 7-74789226-T-C
• gnomAD v4: 7-74789226-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789226T>C , CM000669.2:g.74789226T>C	GRCh38
NC_000007.13:g.74203570T>C , CM000669.1:g.74203570T>C	GRCh37
NC_000007.12:g.73841506T>C	NCBI36
NG_009078.2:g.20263T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*66T>C MANE Select	ENSP00000289473.4:n.*66T>C
ENST00000289473.10:c.*66T>C	ENSP00000289473.4:n.*66T>C
ENST00000289473.8:c.*66T>C	ENSP00000289473.4:n.*66T>C
ENST00000398421.6:n.2266T>C
ENST00000455062.2:n.1348T>C
NM_000265.5:c.*66T>C	NP_000256.4:n.*66T>C
XM_005250543.3:c.*160T>C	XP_005250600.2:n.*160T>C
XM_011516498.1:c.*113T>C	XP_011514800.1:n.*113T>C
XM_011516501.1:c.*66T>C	XP_011514803.1:n.*66T>C
NM_000265.6:c.*66T>C	NP_000256.4:n.*66T>C
NM_000265.7:c.*66T>C MANE Select	NP_000256.4:n.*66T>C