Canonical Allele Identifier: CA2776494886

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789237del , CM000669.2:g.74789237del	GRCh38
NC_000007.13:g.74203581del , CM000669.1:g.74203581del	GRCh37
NC_000007.12:g.73841517del	NCBI36
NG_009078.2:g.20274del

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*77del MANE Select	ENSP00000289473.4:n.*77del
ENST00000289473.10:c.*77del	ENSP00000289473.4:n.*77del
ENST00000289473.8:c.*77del	ENSP00000289473.4:n.*77del
ENST00000398421.6:n.2277del
ENST00000455062.2:n.1359del
NM_000265.5:c.*77del	NP_000256.4:n.*77del
XM_005250543.3:c.*171del	XP_005250600.2:n.*171del
XM_011516498.1:c.*124del	XP_011514800.1:n.*124del
XM_011516501.1:c.*77del	XP_011514803.1:n.*77del
NM_000265.6:c.*77del	NP_000256.4:n.*77del
NM_000265.7:c.*77del MANE Select	NP_000256.4:n.*77del