Canonical Allele Identifier: CA367955893
Gene: NCF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.74203407C>A (hg19) chr7:g.74789063C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789063C>A , CM000669.2:g.74789063C>A GRCh38
NC_000007.13:g.74203407C>A , CM000669.1:g.74203407C>A GRCh37
NC_000007.12:g.73841343C>A NCBI36
NG_009078.2:g.20100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1076C>A MANE Select ENSP00000289473.4:p.Ser359Tyr
ENST00000289473.10:c.1076C>A ENSP00000289473.4:p.Ser359Tyr
ENST00000289473.8:c.1076C>A ENSP00000289473.4:p.Ser359Tyr
ENST00000398421.6:n.2103C>A
ENST00000455062.2:n.1185C>A
NM_000265.5:c.1076C>A NP_000256.4:p.Ser359Tyr
XM_005250543.3:c.1038C>A XP_005250600.2:p.Leu346=
XM_011516498.1:c.1075C>A XP_011514800.1:p.Leu359Ile
XM_011516501.1:c.683C>A XP_011514803.1:p.Ser228Tyr
NM_000265.6:c.1076C>A NP_000256.4:p.Ser359Tyr
NM_000265.7:c.1076C>A MANE Select NP_000256.4:p.Ser359Tyr
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