Canonical Allele Identifier: CA1519920444
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198987G= , CM000666.2:g.186198987G= GRCh38
NC_000004.11:g.187120141G= , CM000666.1:g.187120141G= GRCh37
NC_000004.10:g.187357135G= NCBI36
NG_007965.1:g.12468G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.705G= MANE Select ENSP00000368079.4:p.Lys235=
ENST00000378802.4:c.705G= ENSP00000368079.4:p.Lys235=
ENST00000507209.5:n.1546G=
NM_207352.3:c.705G= NP_997235.3:p.Lys235=
XM_005262935.2:c.705G= XP_005262992.1:p.Lys235=
XM_006714184.2:c.309G= XP_006714247.1:p.Lys103=
XM_005262935.4:c.705G= XP_005262992.1:p.Lys235=
XM_017008037.1:c.309G= XP_016863526.1:p.Lys103=
NM_207352.4:c.705G= MANE Select NP_997235.3:p.Lys235=