Canonical Allele Identifier: CA2764867793

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197144_186197145del , CM000666.2:g.186197144_186197145del	GRCh38
NC_000004.11:g.187118298_187118299del , CM000666.1:g.187118298_187118299del	GRCh37
NC_000004.10:g.187355292_187355293del	NCBI36
NG_007965.1:g.10625_10626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+14_604+15del MANE Select	ENSP00000368079.4:n.604+14_604+15del
ENST00000378802.4:c.604+14_604+15del	ENSP00000368079.4:n.604+14_604+15del
ENST00000507209.5:n.1057_1058del
NM_207352.3:c.604+14_604+15del	NP_997235.3:n.604+14_604+15del
XM_005262935.2:c.604+14_604+15del	XP_005262992.1:n.604+14_604+15del
XM_006714184.2:c.208+14_208+15del	XP_006714247.1:n.208+14_208+15del
XM_005262935.4:c.604+14_604+15del	XP_005262992.1:n.604+14_604+15del
XM_017008037.1:c.208+14_208+15del	XP_016863526.1:n.208+14_208+15del
NM_207352.4:c.604+14_604+15del MANE Select	NP_997235.3:n.604+14_604+15del