Canonical Allele Identifier: CA1103162804

Gene: NCF1

Linked Data

• gnomAD v3: 7-74789196-T-A
• gnomAD v4: 7-74789196-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789196T>A , CM000669.2:g.74789196T>A	GRCh38
NC_000007.13:g.74203540T>A , CM000669.1:g.74203540T>A	GRCh37
NC_000007.12:g.73841476T>A	NCBI36
NG_009078.2:g.20233T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*36T>A MANE Select	ENSP00000289473.4:n.*36T>A
ENST00000289473.10:c.*36T>A	ENSP00000289473.4:n.*36T>A
ENST00000289473.8:c.*36T>A	ENSP00000289473.4:n.*36T>A
ENST00000398421.6:n.2236T>A
ENST00000455062.2:n.1318T>A
NM_000265.5:c.*36T>A	NP_000256.4:n.*36T>A
XM_005250543.3:c.*130T>A	XP_005250600.2:n.*130T>A
XM_011516498.1:c.*83T>A	XP_011514800.1:n.*83T>A
XM_011516501.1:c.*36T>A	XP_011514803.1:n.*36T>A
NM_000265.6:c.*36T>A	NP_000256.4:n.*36T>A
NM_000265.7:c.*36T>A MANE Select	NP_000256.4:n.*36T>A