Canonical Allele Identifier: CA1519891304
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208900A= , CM000666.2:g.186208900A= GRCh38
NC_000004.11:g.187130054A= , CM000666.1:g.187130054A= GRCh37
NC_000004.10:g.187367048A= NCBI36
NG_007965.1:g.22381A=
NG_012095.2:g.4922A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1126A= MANE Select ENSP00000368079.4:p.Lys376=
ENST00000378802.4:c.1126A= ENSP00000368079.4:p.Lys376=
ENST00000502665.1:n.361A=
ENST00000507209.5:n.5824A=
ENST00000513354.5:n.216A=
NM_207352.3:c.1126A= NP_997235.3:p.Lys376=
XM_005262935.2:c.1126A= XP_005262992.1:p.Lys376=
XM_006714184.2:c.730A= XP_006714247.1:p.Lys244=
XM_005262935.4:c.1126A= XP_005262992.1:p.Lys376=
XM_017008037.1:c.730A= XP_016863526.1:p.Lys244=
NM_207352.4:c.1126A= MANE Select NP_997235.3:p.Lys376=