Canonical Allele Identifier: CA1519920379

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736227409

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198835_186198837del , CM000666.2:g.186198835_186198837del	GRCh38
NC_000004.11:g.187119989_187119991del , CM000666.1:g.187119989_187119991del	GRCh37
NC_000004.10:g.187356983_187356985del	NCBI36
NG_007965.1:g.12316_12318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-122_675-120del MANE Select	ENSP00000368079.4:n.675-122_675-120del
ENST00000378802.4:c.675-122_675-120del	ENSP00000368079.4:n.675-122_675-120del
ENST00000507209.5:n.1516-122_1516-120del
NM_207352.3:c.675-122_675-120del	NP_997235.3:n.675-122_675-120del
XM_005262935.2:c.675-122_675-120del	XP_005262992.1:n.675-122_675-120del
XM_006714184.2:c.279-122_279-120del	XP_006714247.1:n.279-122_279-120del
XM_005262935.4:c.675-122_675-120del	XP_005262992.1:n.675-122_675-120del
XM_017008037.1:c.279-122_279-120del	XP_016863526.1:n.279-122_279-120del
NM_207352.4:c.675-122_675-120del MANE Select	NP_997235.3:n.675-122_675-120del