Canonical Allele Identifier: CA1519891324
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208952C= , CM000666.2:g.186208952C= GRCh38
NC_000004.11:g.187130106C= , CM000666.1:g.187130106C= GRCh37
NC_000004.10:g.187367100C= NCBI36
NG_007965.1:g.22433C=
NG_012095.2:g.4974C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1178C= MANE Select ENSP00000368079.4:p.Pro393=
ENST00000378802.4:c.1178C= ENSP00000368079.4:p.Pro393=
ENST00000502665.1:n.413C=
ENST00000507209.5:n.5876C=
ENST00000513354.5:n.268C=
NM_207352.3:c.1178C= NP_997235.3:p.Pro393=
XM_005262935.2:c.1178C= XP_005262992.1:p.Pro393=
XM_006714184.2:c.782C= XP_006714247.1:p.Pro261=
XM_005262935.4:c.1178C= XP_005262992.1:p.Pro393=
XM_017008037.1:c.782C= XP_016863526.1:p.Pro261=
NM_207352.4:c.1178C= MANE Select NP_997235.3:p.Pro393=