Canonical Allele Identifier: CA367953438

Gene: NCF1

Linked Data

• gnomAD v4: 7-74783581-G-T
• MyVariant Identifiers: chr7:g.74197924G>T (hg19) ; chr7:g.74783581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783581G>T , CM000669.2:g.74783581G>T	GRCh38
NC_000007.13:g.74197924G>T , CM000669.1:g.74197924G>T	GRCh37
NC_000007.12:g.73835860G>T	NCBI36
NG_009078.2:g.14618G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.631G>T MANE Select	ENSP00000289473.4:p.Glu211Ter
ENST00000289473.10:c.631G>T	ENSP00000289473.4:p.Glu211Ter
ENST00000289473.8:c.631G>T	ENSP00000289473.4:p.Glu211Ter
ENST00000398421.6:n.1188G>T
ENST00000443956.7:n.752G>T
ENST00000455062.2:n.778G>T
ENST00000464878.5:c.944G>T
ENST00000486097.1:n.139G>T
NM_000265.5:c.631G>T	NP_000256.4:p.Glu211Ter
XM_005250543.3:c.631G>T	XP_005250600.2:p.Glu211Ter
XM_005250544.3:c.631G>T	XP_005250601.2:p.Glu211Ter
XM_011516498.1:c.631G>T	XP_011514800.1:p.Glu211Ter
XM_011516499.1:c.631G>T	XP_011514801.1:p.Glu211Ter
XM_011516500.1:c.631G>T	XP_011514802.1:p.Glu211Ter
XM_011516501.1:c.238G>T	XP_011514803.1:p.Glu80Ter
XR_242262.3:n.686G>T
XR_927515.1:n.686G>T
NM_000265.6:c.631G>T	NP_000256.4:p.Glu211Ter
NM_000265.7:c.631G>T MANE Select	NP_000256.4:p.Glu211Ter