Canonical Allele Identifier: CA2764867704
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204675del , CM000666.2:g.186204675del GRCh38
NC_000004.11:g.187125829del , CM000666.1:g.187125829del GRCh37
NC_000004.10:g.187362823del NCBI36
NG_007965.1:g.18156del
NG_012095.2:g.697del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-525del MANE Select ENSP00000368079.4:n.988-525del
ENST00000378802.4:c.988-525del ENSP00000368079.4:n.988-525del
ENST00000507209.5:n.5161del
ENST00000513354.5:n.77+218del
NM_207352.3:c.988-525del NP_997235.3:n.988-525del
XM_005262935.2:c.988-525del XP_005262992.1:n.988-525del
XM_006714184.2:c.592-525del XP_006714247.1:n.592-525del
XM_005262935.4:c.988-525del XP_005262992.1:n.988-525del
XM_017008037.1:c.592-525del XP_016863526.1:n.592-525del
NM_207352.4:c.988-525del MANE Select NP_997235.3:n.988-525del