Canonical Allele Identifier: CA1519891296
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208883C= , CM000666.2:g.186208883C= GRCh38
NC_000004.11:g.187130037C= , CM000666.1:g.187130037C= GRCh37
NC_000004.10:g.187367031C= NCBI36
NG_007965.1:g.22364C=
NG_012095.2:g.4905C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1109C= MANE Select ENSP00000368079.4:p.Ala370=
ENST00000378802.4:c.1109C= ENSP00000368079.4:p.Ala370=
ENST00000502665.1:n.344C=
ENST00000507209.5:n.5807C=
ENST00000513354.5:n.199C=
NM_207352.3:c.1109C= NP_997235.3:p.Ala370=
XM_005262935.2:c.1109C= XP_005262992.1:p.Ala370=
XM_006714184.2:c.713C= XP_006714247.1:p.Ala238=
XM_005262935.4:c.1109C= XP_005262992.1:p.Ala370=
XM_017008037.1:c.713C= XP_016863526.1:p.Ala238=
NM_207352.4:c.1109C= MANE Select NP_997235.3:p.Ala370=