Canonical Allele Identifier: CA1519919224
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197485A= , CM000666.2:g.186197485A= GRCh38
NC_000004.11:g.187118639A= , CM000666.1:g.187118639A= GRCh37
NC_000004.10:g.187355633A= NCBI36
NG_007965.1:g.10966A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-48A= MANE Select ENSP00000368079.4:n.605-48A=
ENST00000378802.4:c.605-48A= ENSP00000368079.4:n.605-48A=
ENST00000507209.5:n.1398A=
NM_207352.3:c.605-48A= NP_997235.3:n.605-48A=
XM_005262935.2:c.605-48A= XP_005262992.1:n.605-48A=
XM_006714184.2:c.209-48A= XP_006714247.1:n.209-48A=
XM_005262935.4:c.605-48A= XP_005262992.1:n.605-48A=
XM_017008037.1:c.209-48A= XP_016863526.1:n.209-48A=
NM_207352.4:c.605-48A= MANE Select NP_997235.3:n.605-48A=