Canonical Allele Identifier: CA2764867925
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197589_186197590insAGTA , CM000666.2:g.186197589_186197590insAGTA GRCh38
NC_000004.11:g.187118743_187118744insAGTA , CM000666.1:g.187118743_187118744insAGTA GRCh37
NC_000004.10:g.187355737_187355738insAGTA NCBI36
NG_007965.1:g.11070_11071insAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.661_662insAGTA MANE Select ENSP00000368079.4:p.Arg221GlnfsTer2
ENST00000378802.4:c.661_662insAGTA ENSP00000368079.4:p.Arg221GlnfsTer2
ENST00000507209.5:n.1502_1503insAGTA
NM_207352.3:c.661_662insAGTA NP_997235.3:p.Arg221GlnfsTer2
XM_005262935.2:c.661_662insAGTA XP_005262992.1:p.Arg221GlnfsTer2
XM_006714184.2:c.265_266insAGTA XP_006714247.1:p.Arg89GlnfsTer2
XM_005262935.4:c.661_662insAGTA XP_005262992.1:p.Arg221GlnfsTer2
XM_017008037.1:c.265_266insAGTA XP_016863526.1:p.Arg89GlnfsTer2
NM_207352.4:c.661_662insAGTA MANE Select NP_997235.3:p.Arg221GlnfsTer2