Canonical Allele Identifier: CA2764867642
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204635_186204636insGAG , CM000666.2:g.186204635_186204636insGAG GRCh38
NC_000004.11:g.187125789_187125790insGAG , CM000666.1:g.187125789_187125790insGAG GRCh37
NC_000004.10:g.187362783_187362784insGAG NCBI36
NG_007965.1:g.18116_18117insGAG
NG_012095.2:g.657_658insGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-565_988-564insGAG MANE Select ENSP00000368079.4:n.988-565_988-564insGAG
ENST00000378802.4:c.988-565_988-564insGAG ENSP00000368079.4:n.988-565_988-564insGAG
ENST00000507209.5:n.5121_5122insGAG
ENST00000513354.5:n.77+178_77+179insGAG
NM_207352.3:c.988-565_988-564insGAG NP_997235.3:n.988-565_988-564insGAG
XM_005262935.2:c.988-565_988-564insGAG XP_005262992.1:n.988-565_988-564insGAG
XM_006714184.2:c.592-565_592-564insGAG XP_006714247.1:n.592-565_592-564insGAG
XM_005262935.4:c.988-565_988-564insGAG XP_005262992.1:n.988-565_988-564insGAG
XM_017008037.1:c.592-565_592-564insGAG XP_016863526.1:n.592-565_592-564insGAG
NM_207352.4:c.988-565_988-564insGAG MANE Select NP_997235.3:n.988-565_988-564insGAG