Canonical Allele Identifier: CA367955890
Gene: NCF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789062T>G , CM000669.2:g.74789062T>G GRCh38
NC_000007.13:g.74203406T>G , CM000669.1:g.74203406T>G GRCh37
NC_000007.12:g.73841342T>G NCBI36
NG_009078.2:g.20099T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1075T>G MANE Select ENSP00000289473.4:p.Ser359Ala
ENST00000289473.10:c.1075T>G ENSP00000289473.4:p.Ser359Ala
ENST00000289473.8:c.1075T>G ENSP00000289473.4:p.Ser359Ala
ENST00000398421.6:n.2102T>G
ENST00000455062.2:n.1184T>G
NM_000265.5:c.1075T>G NP_000256.4:p.Ser359Ala
XM_005250543.3:c.1037T>G XP_005250600.2:p.Leu346Arg
XM_011516498.1:c.1074T>G XP_011514800.1:p.Ala358=
XM_011516501.1:c.682T>G XP_011514803.1:p.Ser228Ala
NM_000265.6:c.1075T>G NP_000256.4:p.Ser359Ala
NM_000265.7:c.1075T>G MANE Select NP_000256.4:p.Ser359Ala