Canonical Allele Identifier: CA2764867903
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197453del , CM000666.2:g.186197453del GRCh38
NC_000004.11:g.187118607del , CM000666.1:g.187118607del GRCh37
NC_000004.10:g.187355601del NCBI36
NG_007965.1:g.10934del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-80del MANE Select ENSP00000368079.4:n.605-80del
ENST00000378802.4:c.605-80del ENSP00000368079.4:n.605-80del
ENST00000507209.5:n.1366del
NM_207352.3:c.605-80del NP_997235.3:n.605-80del
XM_005262935.2:c.605-80del XP_005262992.1:n.605-80del
XM_006714184.2:c.209-80del XP_006714247.1:n.209-80del
XM_005262935.4:c.605-80del XP_005262992.1:n.605-80del
XM_017008037.1:c.209-80del XP_016863526.1:n.209-80del
NM_207352.4:c.605-80del MANE Select NP_997235.3:n.605-80del