Canonical Allele Identifier: CA842139190

Gene: NCF1

Linked Data

• dbSNP Id: rs1362454457
• MyVariant Identifiers: chr7:g.74783464G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783464G>A , CM000669.2:g.74783464G>A	GRCh38
NC_000007.13:g.74197807G>A , CM000669.1:g.74197807G>A	GRCh37
NC_000007.12:g.73835743G>A	NCBI36
NG_009078.2:g.14501G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.575-61G>A MANE Select	ENSP00000289473.4:n.575-61G>A
ENST00000289473.10:c.575-61G>A	ENSP00000289473.4:n.575-61G>A
ENST00000289473.8:c.575-61G>A	ENSP00000289473.4:n.575-61G>A
ENST00000398421.6:n.1071G>A
ENST00000443956.7:n.696-61G>A
ENST00000449343.6:n.998G>A
ENST00000455062.2:n.661G>A
ENST00000464878.5:c.827G>A
ENST00000486097.1:n.22G>A
NM_000265.5:c.575-61G>A	NP_000256.4:n.575-61G>A
XM_005250543.3:c.575-61G>A	XP_005250600.2:n.575-61G>A
XM_005250544.3:c.575-61G>A	XP_005250601.2:n.575-61G>A
XM_011516498.1:c.575-61G>A	XP_011514800.1:n.575-61G>A
XM_011516499.1:c.575-61G>A	XP_011514801.1:n.575-61G>A
XM_011516500.1:c.575-61G>A	XP_011514802.1:n.575-61G>A
XM_011516501.1:c.182-61G>A	XP_011514803.1:n.182-61G>A
XR_242262.3:n.630-61G>A
XR_927515.1:n.630-61G>A
NM_000265.6:c.575-61G>A	NP_000256.4:n.575-61G>A
NM_000265.7:c.575-61G>A MANE Select	NP_000256.4:n.575-61G>A