Canonical Allele Identifier: CA1519891315
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208931A= , CM000666.2:g.186208931A= GRCh38
NC_000004.11:g.187130085A= , CM000666.1:g.187130085A= GRCh37
NC_000004.10:g.187367079A= NCBI36
NG_007965.1:g.22412A=
NG_012095.2:g.4953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1157A= MANE Select ENSP00000368079.4:p.Lys386=
ENST00000378802.4:c.1157A= ENSP00000368079.4:p.Lys386=
ENST00000502665.1:n.392A=
ENST00000507209.5:n.5855A=
ENST00000513354.5:n.247A=
NM_207352.3:c.1157A= NP_997235.3:p.Lys386=
XM_005262935.2:c.1157A= XP_005262992.1:p.Lys386=
XM_006714184.2:c.761A= XP_006714247.1:p.Lys254=
XM_005262935.4:c.1157A= XP_005262992.1:p.Lys386=
XM_017008037.1:c.761A= XP_016863526.1:p.Lys254=
NM_207352.4:c.1157A= MANE Select NP_997235.3:p.Lys386=