Canonical Allele Identifier: CA1519889022
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205261A= , CM000666.2:g.186205261A= GRCh38
NC_000004.11:g.187126415A= , CM000666.1:g.187126415A= GRCh37
NC_000004.10:g.187363409A= NCBI36
NG_007965.1:g.18742A=
NG_012095.2:g.1283A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1049A= MANE Select ENSP00000368079.4:p.Glu350=
ENST00000378802.4:c.1049A= ENSP00000368079.4:p.Glu350=
ENST00000502665.1:n.284A=
ENST00000507209.5:n.5747A=
ENST00000513354.5:n.139A=
NM_207352.3:c.1049A= NP_997235.3:p.Glu350=
XM_005262935.2:c.1049A= XP_005262992.1:p.Glu350=
XM_006714184.2:c.653A= XP_006714247.1:p.Glu218=
XM_005262935.4:c.1049A= XP_005262992.1:p.Glu350=
XM_017008037.1:c.653A= XP_016863526.1:p.Glu218=
NM_207352.4:c.1049A= MANE Select NP_997235.3:p.Glu350=