Canonical Allele Identifier: CA1519891501
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209265C= , CM000666.2:g.186209265C= GRCh38
NC_000004.11:g.187130419C= , CM000666.1:g.187130419C= GRCh37
NC_000004.10:g.187367413C= NCBI36
NG_007965.1:g.22746C=
NG_012095.2:g.5287C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1398C= MANE Select ENSP00000368079.4:p.Asn466=
ENST00000378802.4:c.1398C= ENSP00000368079.4:p.Asn466=
ENST00000502665.1:n.633C=
ENST00000507209.5:n.6096C=
ENST00000511608.5:n.194C=
ENST00000513354.5:n.488C=
NM_207352.3:c.1398C= NP_997235.3:p.Asn466=
XM_005262935.2:c.1395C= XP_005262992.1:p.Asn465=
XM_006714184.2:c.1002C= XP_006714247.1:p.Asn334=
XM_005262935.4:c.1395C= XP_005262992.1:p.Asn465=
XM_017008037.1:c.1002C= XP_016863526.1:p.Asn334=
NM_207352.4:c.1398C= MANE Select NP_997235.3:p.Asn466=