Canonical Allele Identifier: CA2324927424
Gene: CYP4F22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540617_15540618delinsAG , CM000681.2:g.15540617_15540618delinsAG GRCh38
NC_000019.9:g.15651428_15651429delinsAG , CM000681.1:g.15651428_15651429delinsAG GRCh37
NC_000019.8:g.15512428_15512429delinsAG NCBI36
NG_007987.1:g.37093_37094delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.839_840delinsAG MANE Select ENSP00000269703.1:p.Gln280=
ENST00000269703.7:c.839_840delinsAG ENSP00000269703.1:p.Gln280=
ENST00000601005.2:c.839_840delinsAG ENSP00000469866.1:p.Gln280=
NM_173483.3:c.839_840delinsAG NP_775754.2:p.Gln280=
XM_011527692.1:c.839_840delinsAG XP_011525994.1:p.Gln280=
XM_011527693.1:c.839_840delinsAG XP_011525995.1:p.Gln280=
XM_011527692.2:c.839_840delinsAG XP_011525994.1:p.Gln280=
XM_011527693.2:c.839_840delinsAG XP_011525995.1:p.Gln280=
NM_173483.4:c.839_840delinsAG MANE Select NP_775754.2:p.Gln280=
Search 100 bp 5'
Search 100 bp 3'