Canonical Allele Identifier: CA1519891298
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208888G= , CM000666.2:g.186208888G= GRCh38
NC_000004.11:g.187130042G= , CM000666.1:g.187130042G= GRCh37
NC_000004.10:g.187367036G= NCBI36
NG_007965.1:g.22369G=
NG_012095.2:g.4910G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1114G= MANE Select ENSP00000368079.4:p.Val372=
ENST00000378802.4:c.1114G= ENSP00000368079.4:p.Val372=
ENST00000502665.1:n.349G=
ENST00000507209.5:n.5812G=
ENST00000513354.5:n.204G=
NM_207352.3:c.1114G= NP_997235.3:p.Val372=
XM_005262935.2:c.1114G= XP_005262992.1:p.Val372=
XM_006714184.2:c.718G= XP_006714247.1:p.Val240=
XM_005262935.4:c.1114G= XP_005262992.1:p.Val372=
XM_017008037.1:c.718G= XP_016863526.1:p.Val240=
NM_207352.4:c.1114G= MANE Select NP_997235.3:p.Val372=