Canonical Allele Identifier: CA1519891504
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209271A= , CM000666.2:g.186209271A= GRCh38
NC_000004.11:g.187130425A= , CM000666.1:g.187130425A= GRCh37
NC_000004.10:g.187367419A= NCBI36
NG_007965.1:g.22752A=
NG_012095.2:g.5293A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1404A= MANE Select ENSP00000368079.4:p.Ile468=
ENST00000378802.4:c.1404A= ENSP00000368079.4:p.Ile468=
ENST00000502665.1:n.639A=
ENST00000507209.5:n.6102A=
ENST00000511608.5:n.200A=
ENST00000513354.5:n.494A=
NM_207352.3:c.1404A= NP_997235.3:p.Ile468=
XM_005262935.2:c.1401A= XP_005262992.1:p.Ile467=
XM_006714184.2:c.1008A= XP_006714247.1:p.Ile336=
XM_005262935.4:c.1401A= XP_005262992.1:p.Ile467=
XM_017008037.1:c.1008A= XP_016863526.1:p.Ile336=
NM_207352.4:c.1404A= MANE Select NP_997235.3:p.Ile468=