Canonical Allele Identifier: CA2764868255

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205472_186205476del , CM000666.2:g.186205472_186205476del	GRCh38
NC_000004.11:g.187126626_187126630del , CM000666.1:g.187126626_187126630del	GRCh37
NC_000004.10:g.187363620_187363624del	NCBI36
NG_007965.1:g.18953_18957del
NG_012095.2:g.1494_1498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+170_1090+174del MANE Select	ENSP00000368079.4:n.1090+170_1090+174del
ENST00000378802.4:c.1090+170_1090+174del	ENSP00000368079.4:n.1090+170_1090+174del
ENST00000502665.1:n.325+170_325+174del
ENST00000507209.5:n.5788+170_5788+174del
ENST00000513354.5:n.180+170_180+174del
NM_207352.3:c.1090+170_1090+174del	NP_997235.3:n.1090+170_1090+174del
XM_005262935.2:c.1090+170_1090+174del	XP_005262992.1:n.1090+170_1090+174del
XM_006714184.2:c.694+170_694+174del	XP_006714247.1:n.694+170_694+174del
XM_005262935.4:c.1090+170_1090+174del	XP_005262992.1:n.1090+170_1090+174del
XM_017008037.1:c.694+170_694+174del	XP_016863526.1:n.694+170_694+174del
NM_207352.4:c.1090+170_1090+174del MANE Select	NP_997235.3:n.1090+170_1090+174del