Canonical Allele Identifier: CA1519919406
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197593C= , CM000666.2:g.186197593C= GRCh38
NC_000004.11:g.187118747C= , CM000666.1:g.187118747C= GRCh37
NC_000004.10:g.187355741C= NCBI36
NG_007965.1:g.11074C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.665C= MANE Select ENSP00000368079.4:p.Ala222=
ENST00000378802.4:c.665C= ENSP00000368079.4:p.Ala222=
ENST00000507209.5:n.1506C=
NM_207352.3:c.665C= NP_997235.3:p.Ala222=
XM_005262935.2:c.665C= XP_005262992.1:p.Ala222=
XM_006714184.2:c.269C= XP_006714247.1:p.Ala90=
XM_005262935.4:c.665C= XP_005262992.1:p.Ala222=
XM_017008037.1:c.269C= XP_016863526.1:p.Ala90=
NM_207352.4:c.665C= MANE Select NP_997235.3:p.Ala222=