Canonical Allele Identifier: CA2764868235

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205441_186205442insA , CM000666.2:g.186205441_186205442insA	GRCh38
NC_000004.11:g.187126595_187126596insA , CM000666.1:g.187126595_187126596insA	GRCh37
NC_000004.10:g.187363589_187363590insA	NCBI36
NG_007965.1:g.18922_18923insA
NG_012095.2:g.1463_1464insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+139_1090+140insA MANE Select	ENSP00000368079.4:n.1090+139_1090+140insA
ENST00000378802.4:c.1090+139_1090+140insA	ENSP00000368079.4:n.1090+139_1090+140insA
ENST00000502665.1:n.325+139_325+140insA
ENST00000507209.5:n.5788+139_5788+140insA
ENST00000513354.5:n.180+139_180+140insA
NM_207352.3:c.1090+139_1090+140insA	NP_997235.3:n.1090+139_1090+140insA
XM_005262935.2:c.1090+139_1090+140insA	XP_005262992.1:n.1090+139_1090+140insA
XM_006714184.2:c.694+139_694+140insA	XP_006714247.1:n.694+139_694+140insA
XM_005262935.4:c.1090+139_1090+140insA	XP_005262992.1:n.1090+139_1090+140insA
XM_017008037.1:c.694+139_694+140insA	XP_016863526.1:n.694+139_694+140insA
NM_207352.4:c.1090+139_1090+140insA MANE Select	NP_997235.3:n.1090+139_1090+140insA