Canonical Allele Identifier: CA367953609

Gene: NCF1

Linked Data

• MyVariant Identifiers: chr7:g.74197967A>T (hg19) ; chr7:g.74783624A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783624A>T , CM000669.2:g.74783624A>T	GRCh38
NC_000007.13:g.74197967A>T , CM000669.1:g.74197967A>T	GRCh37
NC_000007.12:g.73835903A>T	NCBI36
NG_009078.2:g.14661A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.674A>T MANE Select	ENSP00000289473.4:p.Asn225Ile
ENST00000289473.10:c.674A>T	ENSP00000289473.4:p.Asn225Ile
ENST00000289473.8:c.674A>T	ENSP00000289473.4:p.Asn225Ile
ENST00000398421.6:n.1231A>T
ENST00000443956.7:n.795A>T
ENST00000455062.2:n.821A>T
ENST00000486097.1:n.182A>T
NM_000265.5:c.674A>T	NP_000256.4:p.Asn225Ile
XM_005250543.3:c.674A>T	XP_005250600.2:p.Asn225Ile
XM_005250544.3:c.674A>T	XP_005250601.2:p.Asn225Ile
XM_011516498.1:c.674A>T	XP_011514800.1:p.Asn225Ile
XM_011516499.1:c.674A>T	XP_011514801.1:p.Asn225Ile
XM_011516500.1:c.674A>T	XP_011514802.1:p.Asn225Ile
XM_011516501.1:c.281A>T	XP_011514803.1:p.Asn94Ile
XR_242262.3:n.729A>T
XR_927515.1:n.729A>T
NM_000265.6:c.674A>T	NP_000256.4:p.Asn225Ile
NM_000265.7:c.674A>T MANE Select	NP_000256.4:p.Asn225Ile