Canonical Allele Identifier: CA1519918622
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197090_186197091delinsCT , CM000666.2:g.186197090_186197091delinsCT GRCh38
NC_000004.11:g.187118244_187118245delinsCT , CM000666.1:g.187118244_187118245delinsCT GRCh37
NC_000004.10:g.187355238_187355239delinsCT NCBI36
NG_007965.1:g.10571_10572delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.564_565delinsCT MANE Select ENSP00000368079.4:p.Cys188=
ENST00000378802.4:c.564_565delinsCT ENSP00000368079.4:p.Cys188=
ENST00000507209.5:n.1003_1004delinsCT
NM_207352.3:c.564_565delinsCT NP_997235.3:p.Cys188=
XM_005262935.2:c.564_565delinsCT XP_005262992.1:p.Cys188=
XM_006714184.2:c.168_169delinsCT XP_006714247.1:p.Cys56=
XM_005262935.4:c.564_565delinsCT XP_005262992.1:p.Cys188=
XM_017008037.1:c.168_169delinsCT XP_016863526.1:p.Cys56=
NM_207352.4:c.564_565delinsCT MANE Select NP_997235.3:p.Cys188=
Search 100 bp 5'
Search 100 bp 3'