Canonical Allele Identifier: CA1717692917

Gene: NCF1

Linked Data

• dbSNP Id: rs1796728773

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789003_74789004insCAGT , CM000669.2:g.74789003_74789004insCAGT	GRCh38
NC_000007.13:g.74203347_74203348insCAGT , CM000669.1:g.74203347_74203348insCAGT	GRCh37
NC_000007.12:g.73841283_73841284insCAGT	NCBI36
NG_009078.2:g.20040_20041insCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-36_1052-35insCAGT MANE Select	ENSP00000289473.4:n.1052-36_1052-35insCAGT
ENST00000289473.10:c.1052-36_1052-35insCAGT	ENSP00000289473.4:n.1052-36_1052-35insCAGT
ENST00000289473.8:c.1052-36_1052-35insCAGT	ENSP00000289473.4:n.1052-36_1052-35insCAGT
ENST00000398421.6:n.2079-36_2079-35insCAGT
ENST00000455062.2:n.1161-36_1161-35insCAGT
NM_000265.5:c.1052-36_1052-35insCAGT	NP_000256.4:n.1052-36_1052-35insCAGT
XM_005250543.3:c.1014-36_1014-35insCAGT	XP_005250600.2:n.1014-36_1014-35insCAGT
XM_011516498.1:c.1051-36_1051-35insCAGT	XP_011514800.1:n.1051-36_1051-35insCAGT
XM_011516501.1:c.659-36_659-35insCAGT	XP_011514803.1:n.659-36_659-35insCAGT
NM_000265.6:c.1052-36_1052-35insCAGT	NP_000256.4:n.1052-36_1052-35insCAGT
NM_000265.7:c.1052-36_1052-35insCAGT MANE Select	NP_000256.4:n.1052-36_1052-35insCAGT