Canonical Allele Identifier: CA1519889013
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205251T= , CM000666.2:g.186205251T= GRCh38
NC_000004.11:g.187126405T= , CM000666.1:g.187126405T= GRCh37
NC_000004.10:g.187363399T= NCBI36
NG_007965.1:g.18732T=
NG_012095.2:g.1273T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1039T= MANE Select ENSP00000368079.4:p.Ser347=
ENST00000378802.4:c.1039T= ENSP00000368079.4:p.Ser347=
ENST00000502665.1:n.274T=
ENST00000507209.5:n.5737T=
ENST00000513354.5:n.129T=
NM_207352.3:c.1039T= NP_997235.3:p.Ser347=
XM_005262935.2:c.1039T= XP_005262992.1:p.Ser347=
XM_006714184.2:c.643T= XP_006714247.1:p.Ser215=
XM_005262935.4:c.1039T= XP_005262992.1:p.Ser347=
XM_017008037.1:c.643T= XP_016863526.1:p.Ser215=
NM_207352.4:c.1039T= MANE Select NP_997235.3:p.Ser347=