Canonical Allele Identifier: CA2578249649

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198947_186198948del , CM000666.2:g.186198947_186198948del	GRCh38
NC_000004.11:g.187120101_187120102del , CM000666.1:g.187120101_187120102del	GRCh37
NC_000004.10:g.187357095_187357096del	NCBI36
NG_007965.1:g.12428_12429del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.675-10_675-9del MANE Select	ENSP00000368079.4:n.675-10_675-9del
ENST00000378802.4:c.675-10_675-9del	ENSP00000368079.4:n.675-10_675-9del
ENST00000507209.5:n.1516-10_1516-9del
NM_207352.3:c.675-10_675-9del	NP_997235.3:n.675-10_675-9del
XM_005262935.2:c.675-10_675-9del	XP_005262992.1:n.675-10_675-9del
XM_006714184.2:c.279-10_279-9del	XP_006714247.1:n.279-10_279-9del
XM_005262935.4:c.675-10_675-9del	XP_005262992.1:n.675-10_675-9del
XM_017008037.1:c.279-10_279-9del	XP_016863526.1:n.279-10_279-9del
NM_207352.4:c.675-10_675-9del MANE Select	NP_997235.3:n.675-10_675-9del