Canonical Allele Identifier: CA1519920307

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198662_186198664delinsCAG , CM000666.2:g.186198662_186198664delinsCAG	GRCh38
NC_000004.11:g.187119816_187119818delinsCAG , CM000666.1:g.187119816_187119818delinsCAG	GRCh37
NC_000004.10:g.187356810_187356812delinsCAG	NCBI36
NG_007965.1:g.12143_12145delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-295_675-293delinsCAG MANE Select	ENSP00000368079.4:n.675-295_675-293delinsCAG
ENST00000378802.4:c.675-295_675-293delinsCAG	ENSP00000368079.4:n.675-295_675-293delinsCAG
ENST00000507209.5:n.1516-295_1516-293delinsCAG
NM_207352.3:c.675-295_675-293delinsCAG	NP_997235.3:n.675-295_675-293delinsCAG
XM_005262935.2:c.675-295_675-293delinsCAG	XP_005262992.1:n.675-295_675-293delinsCAG
XM_006714184.2:c.279-295_279-293delinsCAG	XP_006714247.1:n.279-295_279-293delinsCAG
XM_005262935.4:c.675-295_675-293delinsCAG	XP_005262992.1:n.675-295_675-293delinsCAG
XM_017008037.1:c.279-295_279-293delinsCAG	XP_016863526.1:n.279-295_279-293delinsCAG
NM_207352.4:c.675-295_675-293delinsCAG MANE Select	NP_997235.3:n.675-295_675-293delinsCAG