Canonical Allele Identifier: CA2672897891

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186198848-AATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198852_186198854del , CM000666.2:g.186198852_186198854del	GRCh38
NC_000004.11:g.187120006_187120008del , CM000666.1:g.187120006_187120008del	GRCh37
NC_000004.10:g.187357000_187357002del	NCBI36
NG_007965.1:g.12333_12335del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.675-105_675-103del MANE Select	ENSP00000368079.4:n.675-105_675-103del
ENST00000378802.4:c.675-105_675-103del	ENSP00000368079.4:n.675-105_675-103del
ENST00000507209.5:n.1516-105_1516-103del
NM_207352.3:c.675-105_675-103del	NP_997235.3:n.675-105_675-103del
XM_005262935.2:c.675-105_675-103del	XP_005262992.1:n.675-105_675-103del
XM_006714184.2:c.279-105_279-103del	XP_006714247.1:n.279-105_279-103del
XM_005262935.4:c.675-105_675-103del	XP_005262992.1:n.675-105_675-103del
XM_017008037.1:c.279-105_279-103del	XP_016863526.1:n.279-105_279-103del
NM_207352.4:c.675-105_675-103del MANE Select	NP_997235.3:n.675-105_675-103del