Canonical Allele Identifier: CA1519918274
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186196949_186196953delinsCAAAT , CM000666.2:g.186196949_186196953delinsCAAAT GRCh38
NC_000004.11:g.187118103_187118107delinsCAAAT , CM000666.1:g.187118103_187118107delinsCAAAT GRCh37
NC_000004.10:g.187355097_187355101delinsCAAAT NCBI36
NG_007965.1:g.10430_10434delinsCAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.423_427delinsCAAAT MANE Select ENSP00000368079.4:p.Asn141=
ENST00000378802.4:c.423_427delinsCAAAT ENSP00000368079.4:p.Asn141=
ENST00000507209.5:n.862_866delinsCAAAT
NM_207352.3:c.423_427delinsCAAAT NP_997235.3:p.Asn141=
XM_005262935.2:c.423_427delinsCAAAT XP_005262992.1:p.Asn141=
XM_006714184.2:c.27_31delinsCAAAT XP_006714247.1:p.Asn9=
XM_005262935.4:c.423_427delinsCAAAT XP_005262992.1:p.Asn141=
XM_017008037.1:c.27_31delinsCAAAT XP_016863526.1:p.Asn9=
NM_207352.4:c.423_427delinsCAAAT MANE Select NP_997235.3:p.Asn141=
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