Canonical Allele Identifier: CA358950242
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208954T>A , CM000666.2:g.186208954T>A GRCh38
NC_000004.11:g.187130108T>A , CM000666.1:g.187130108T>A GRCh37
NC_000004.10:g.187367102T>A NCBI36
NG_007965.1:g.22435T>A
NG_012095.2:g.4976T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1180T>A MANE Select ENSP00000368079.4:p.Ser394Thr
ENST00000378802.4:c.1180T>A ENSP00000368079.4:p.Ser394Thr
ENST00000502665.1:n.415T>A
ENST00000507209.5:n.5878T>A
ENST00000513354.5:n.270T>A
NM_207352.3:c.1180T>A NP_997235.3:p.Ser394Thr
XM_005262935.2:c.1180T>A XP_005262992.1:p.Ser394Thr
XM_006714184.2:c.784T>A XP_006714247.1:p.Ser262Thr
XM_005262935.4:c.1180T>A XP_005262992.1:p.Ser394Thr
XM_017008037.1:c.784T>A XP_016863526.1:p.Ser262Thr
NM_207352.4:c.1180T>A MANE Select NP_997235.3:p.Ser394Thr