Canonical Allele Identifier: CA2842537785

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199107del , CM000666.2:g.186199107del	GRCh38
NC_000004.11:g.187120261del , CM000666.1:g.187120261del	GRCh37
NC_000004.10:g.187357255del	NCBI36
NG_007965.1:g.12588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+24del MANE Select	ENSP00000368079.4:n.801+24del
ENST00000378802.4:c.801+24del	ENSP00000368079.4:n.801+24del
ENST00000507209.5:n.1642+24del
NM_207352.3:c.801+24del	NP_997235.3:n.801+24del
XM_005262935.2:c.801+24del	XP_005262992.1:n.801+24del
XM_006714184.2:c.405+24del	XP_006714247.1:n.405+24del
XM_005262935.4:c.801+24del	XP_005262992.1:n.801+24del
XM_017008037.1:c.405+24del	XP_016863526.1:n.405+24del
NM_207352.4:c.801+24del MANE Select	NP_997235.3:n.801+24del