Canonical Allele Identifier: CA1519891288
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208871C= , CM000666.2:g.186208871C= GRCh38
NC_000004.11:g.187130025C= , CM000666.1:g.187130025C= GRCh37
NC_000004.10:g.187367019C= NCBI36
NG_007965.1:g.22352C=
NG_012095.2:g.4893C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1097C= MANE Select ENSP00000368079.4:p.Ser366=
ENST00000378802.4:c.1097C= ENSP00000368079.4:p.Ser366=
ENST00000502665.1:n.332C=
ENST00000507209.5:n.5795C=
ENST00000513354.5:n.187C=
NM_207352.3:c.1097C= NP_997235.3:p.Ser366=
XM_005262935.2:c.1097C= XP_005262992.1:p.Ser366=
XM_006714184.2:c.701C= XP_006714247.1:p.Ser234=
XM_005262935.4:c.1097C= XP_005262992.1:p.Ser366=
XM_017008037.1:c.701C= XP_016863526.1:p.Ser234=
NM_207352.4:c.1097C= MANE Select NP_997235.3:p.Ser366=