Canonical Allele Identifier: CA2578927863

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783497C>T , CM000669.2:g.74783497C>T	GRCh38
NC_000007.13:g.74197840C>T , CM000669.1:g.74197840C>T	GRCh37
NC_000007.12:g.73835776C>T	NCBI36
NG_009078.2:g.14534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.575-28C>T MANE Select	ENSP00000289473.4:n.575-28C>T
ENST00000289473.10:c.575-28C>T	ENSP00000289473.4:n.575-28C>T
ENST00000289473.8:c.575-28C>T	ENSP00000289473.4:n.575-28C>T
ENST00000398421.6:n.1104C>T
ENST00000443956.7:n.696-28C>T
ENST00000449343.6:n.1031C>T
ENST00000455062.2:n.694C>T
ENST00000464878.5:c.860C>T
ENST00000486097.1:n.55C>T
NM_000265.5:c.575-28C>T	NP_000256.4:n.575-28C>T
XM_005250543.3:c.575-28C>T	XP_005250600.2:n.575-28C>T
XM_005250544.3:c.575-28C>T	XP_005250601.2:n.575-28C>T
XM_011516498.1:c.575-28C>T	XP_011514800.1:n.575-28C>T
XM_011516499.1:c.575-28C>T	XP_011514801.1:n.575-28C>T
XM_011516500.1:c.575-28C>T	XP_011514802.1:n.575-28C>T
XM_011516501.1:c.182-28C>T	XP_011514803.1:n.182-28C>T
XR_242262.3:n.630-28C>T
XR_927515.1:n.630-28C>T
NM_000265.6:c.575-28C>T	NP_000256.4:n.575-28C>T
NM_000265.7:c.575-28C>T MANE Select	NP_000256.4:n.575-28C>T