Canonical Allele Identifier: CA2764867863
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204789_186204790insA , CM000666.2:g.186204789_186204790insA GRCh38
NC_000004.11:g.187125943_187125944insA , CM000666.1:g.187125943_187125944insA GRCh37
NC_000004.10:g.187362937_187362938insA NCBI36
NG_007965.1:g.18270_18271insA
NG_012095.2:g.811_812insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-411_988-410insA MANE Select ENSP00000368079.4:n.988-411_988-410insA
ENST00000378802.4:c.988-411_988-410insA ENSP00000368079.4:n.988-411_988-410insA
ENST00000507209.5:n.5275_5276insA
ENST00000513354.5:n.77+332_77+333insA
NM_207352.3:c.988-411_988-410insA NP_997235.3:n.988-411_988-410insA
XM_005262935.2:c.988-411_988-410insA XP_005262992.1:n.988-411_988-410insA
XM_006714184.2:c.592-411_592-410insA XP_006714247.1:n.592-411_592-410insA
XM_005262935.4:c.988-411_988-410insA XP_005262992.1:n.988-411_988-410insA
XM_017008037.1:c.592-411_592-410insA XP_016863526.1:n.592-411_592-410insA
NM_207352.4:c.988-411_988-410insA MANE Select NP_997235.3:n.988-411_988-410insA