Canonical Allele Identifier: CA1519891502
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209267G= , CM000666.2:g.186209267G= GRCh38
NC_000004.11:g.187130421G= , CM000666.1:g.187130421G= GRCh37
NC_000004.10:g.187367415G= NCBI36
NG_007965.1:g.22748G=
NG_012095.2:g.5289G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1400G= MANE Select ENSP00000368079.4:p.Cys467=
ENST00000378802.4:c.1400G= ENSP00000368079.4:p.Cys467=
ENST00000502665.1:n.635G=
ENST00000507209.5:n.6098G=
ENST00000511608.5:n.196G=
ENST00000513354.5:n.490G=
NM_207352.3:c.1400G= NP_997235.3:p.Cys467=
XM_005262935.2:c.1397G= XP_005262992.1:p.Cys466=
XM_006714184.2:c.1004G= XP_006714247.1:p.Cys335=
XM_005262935.4:c.1397G= XP_005262992.1:p.Cys466=
XM_017008037.1:c.1004G= XP_016863526.1:p.Cys335=
NM_207352.4:c.1400G= MANE Select NP_997235.3:p.Cys467=