Canonical Allele Identifier: CA1519891513
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209300C= , CM000666.2:g.186209300C= GRCh38
NC_000004.11:g.187130454C= , CM000666.1:g.187130454C= GRCh37
NC_000004.10:g.187367448C= NCBI36
NG_007965.1:g.22781C=
NG_012095.2:g.5322C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1405+28C= MANE Select ENSP00000368079.4:p.=
ENST00000378802.4:c.1405+28C= ENSP00000368079.4:p.=
ENST00000502665.1:n.640+28C=
ENST00000507209.5:n.6103+28C=
ENST00000511608.5:n.201+28C=
ENST00000513354.5:n.495+28C=
NM_207352.3:c.1405+28C= NP_997235.3:p.=
XM_005262935.2:c.1402+28C= XP_005262992.1:p.=
XM_006714184.2:c.1009+28C= XP_006714247.1:p.=
XM_005262935.4:c.1402+28C= XP_005262992.1:p.=
XM_017008037.1:c.1009+28C= XP_016863526.1:p.=
NM_207352.4:c.1405+28C= MANE Select NP_997235.3:p.=