Canonical Allele Identifier: CA1519920308

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736223713
• gnomAD v3: 4-186198662-CAG-C
• gnomAD v4: 4-186198662-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198665_186198666del , CM000666.2:g.186198665_186198666del	GRCh38
NC_000004.11:g.187119819_187119820del , CM000666.1:g.187119819_187119820del	GRCh37
NC_000004.10:g.187356813_187356814del	NCBI36
NG_007965.1:g.12146_12147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-292_675-291del MANE Select	ENSP00000368079.4:n.675-292_675-291del
ENST00000378802.4:c.675-292_675-291del	ENSP00000368079.4:n.675-292_675-291del
ENST00000507209.5:n.1516-292_1516-291del
NM_207352.3:c.675-292_675-291del	NP_997235.3:n.675-292_675-291del
XM_005262935.2:c.675-292_675-291del	XP_005262992.1:n.675-292_675-291del
XM_006714184.2:c.279-292_279-291del	XP_006714247.1:n.279-292_279-291del
XM_005262935.4:c.675-292_675-291del	XP_005262992.1:n.675-292_675-291del
XM_017008037.1:c.279-292_279-291del	XP_016863526.1:n.279-292_279-291del
NM_207352.4:c.675-292_675-291del MANE Select	NP_997235.3:n.675-292_675-291del