Canonical Allele Identifier: CA2764867981

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205353_186205357del , CM000666.2:g.186205353_186205357del	GRCh38
NC_000004.11:g.187126507_187126511del , CM000666.1:g.187126507_187126511del	GRCh37
NC_000004.10:g.187363501_187363505del	NCBI36
NG_007965.1:g.18834_18838del
NG_012095.2:g.1375_1379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+51_1090+55del MANE Select	ENSP00000368079.4:n.1090+51_1090+55del
ENST00000378802.4:c.1090+51_1090+55del	ENSP00000368079.4:n.1090+51_1090+55del
ENST00000502665.1:n.325+51_325+55del
ENST00000507209.5:n.5788+51_5788+55del
ENST00000513354.5:n.180+51_180+55del
NM_207352.3:c.1090+51_1090+55del	NP_997235.3:n.1090+51_1090+55del
XM_005262935.2:c.1090+51_1090+55del	XP_005262992.1:n.1090+51_1090+55del
XM_006714184.2:c.694+51_694+55del	XP_006714247.1:n.694+51_694+55del
XM_005262935.4:c.1090+51_1090+55del	XP_005262992.1:n.1090+51_1090+55del
XM_017008037.1:c.694+51_694+55del	XP_016863526.1:n.694+51_694+55del
NM_207352.4:c.1090+51_1090+55del MANE Select	NP_997235.3:n.1090+51_1090+55del