Canonical Allele Identifier: CA1519888973
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205217A= , CM000666.2:g.186205217A= GRCh38
NC_000004.11:g.187126371A= , CM000666.1:g.187126371A= GRCh37
NC_000004.10:g.187363365A= NCBI36
NG_007965.1:g.18698A=
NG_012095.2:g.1239A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1005A= MANE Select ENSP00000368079.4:p.Ala335=
ENST00000378802.4:c.1005A= ENSP00000368079.4:p.Ala335=
ENST00000502665.1:n.240A=
ENST00000507209.5:n.5703A=
ENST00000513354.5:n.95A=
NM_207352.3:c.1005A= NP_997235.3:p.Ala335=
XM_005262935.2:c.1005A= XP_005262992.1:p.Ala335=
XM_006714184.2:c.609A= XP_006714247.1:p.Ala203=
XM_005262935.4:c.1005A= XP_005262992.1:p.Ala335=
XM_017008037.1:c.609A= XP_016863526.1:p.Ala203=
NM_207352.4:c.1005A= MANE Select NP_997235.3:p.Ala335=