Canonical Allele Identifier: CA557395940
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1561431918

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186196950_186196953del , CM000666.2:g.186196950_186196953del GRCh38
NC_000004.11:g.187118104_187118107del , CM000666.1:g.187118104_187118107del GRCh37
NC_000004.10:g.187355098_187355101del NCBI36
NG_007965.1:g.10431_10434del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.424_427del MANE Select ENSP00000368079.4:p.Lys142GlyfsTer8
ENST00000378802.4:c.424_427del ENSP00000368079.4:p.Lys142GlyfsTer8
ENST00000507209.5:n.863_866del
NM_207352.3:c.424_427del NP_997235.3:p.Lys142GlyfsTer8
XM_005262935.2:c.424_427del XP_005262992.1:p.Lys142GlyfsTer8
XM_006714184.2:c.28_31del XP_006714247.1:p.Lys10GlyfsTer8
XM_005262935.4:c.424_427del XP_005262992.1:p.Lys142GlyfsTer8
XM_017008037.1:c.28_31del XP_016863526.1:p.Lys10GlyfsTer8
NM_207352.4:c.424_427del MANE Select NP_997235.3:p.Lys142GlyfsTer8