Canonical Allele Identifier: CA358949868
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208867A>G , CM000666.2:g.186208867A>G GRCh38
NC_000004.11:g.187130021A>G , CM000666.1:g.187130021A>G GRCh37
NC_000004.10:g.187367015A>G NCBI36
NG_007965.1:g.22348A>G
NG_012095.2:g.4889A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1093A>G MANE Select ENSP00000368079.4:p.Lys365Glu
ENST00000378802.4:c.1093A>G ENSP00000368079.4:p.Lys365Glu
ENST00000502665.1:n.328A>G
ENST00000507209.5:n.5791A>G
ENST00000513354.5:n.183A>G
NM_207352.3:c.1093A>G NP_997235.3:p.Lys365Glu
XM_005262935.2:c.1093A>G XP_005262992.1:p.Lys365Glu
XM_006714184.2:c.697A>G XP_006714247.1:p.Lys233Glu
XM_005262935.4:c.1093A>G XP_005262992.1:p.Lys365Glu
XM_017008037.1:c.697A>G XP_016863526.1:p.Lys233Glu
NM_207352.4:c.1093A>G MANE Select NP_997235.3:p.Lys365Glu