Canonical Allele Identifier: CA1519891258
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208825A= , CM000666.2:g.186208825A= GRCh38
NC_000004.11:g.187129979A= , CM000666.1:g.187129979A= GRCh37
NC_000004.10:g.187366973A= NCBI36
NG_007965.1:g.22306A=
NG_012095.2:g.4847A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1091-40A= MANE Select ENSP00000368079.4:n.1091-40A=
ENST00000378802.4:c.1091-40A= ENSP00000368079.4:n.1091-40A=
ENST00000502665.1:n.326-40A=
ENST00000507209.5:n.5789-40A=
ENST00000513354.5:n.181-40A=
NM_207352.3:c.1091-40A= NP_997235.3:n.1091-40A=
XM_005262935.2:c.1091-40A= XP_005262992.1:n.1091-40A=
XM_006714184.2:c.695-40A= XP_006714247.1:n.695-40A=
XM_005262935.4:c.1091-40A= XP_005262992.1:n.1091-40A=
XM_017008037.1:c.695-40A= XP_016863526.1:n.695-40A=
NM_207352.4:c.1091-40A= MANE Select NP_997235.3:n.1091-40A=