Canonical Allele Identifier: CA1519891281
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208861T= , CM000666.2:g.186208861T= GRCh38
NC_000004.11:g.187130015T= , CM000666.1:g.187130015T= GRCh37
NC_000004.10:g.187367009T= NCBI36
NG_007965.1:g.22342T=
NG_012095.2:g.4883T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1091-4T= MANE Select ENSP00000368079.4:n.1091-4T=
ENST00000378802.4:c.1091-4T= ENSP00000368079.4:n.1091-4T=
ENST00000502665.1:n.326-4T=
ENST00000507209.5:n.5789-4T=
ENST00000513354.5:n.181-4T=
NM_207352.3:c.1091-4T= NP_997235.3:n.1091-4T=
XM_005262935.2:c.1091-4T= XP_005262992.1:n.1091-4T=
XM_006714184.2:c.695-4T= XP_006714247.1:n.695-4T=
XM_005262935.4:c.1091-4T= XP_005262992.1:n.1091-4T=
XM_017008037.1:c.695-4T= XP_016863526.1:n.695-4T=
NM_207352.4:c.1091-4T= MANE Select NP_997235.3:n.1091-4T=