Canonical Allele Identifier: CA1519891286

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208868_186208869delinsAG , CM000666.2:g.186208868_186208869delinsAG	GRCh38
NC_000004.11:g.187130022_187130023delinsAG , CM000666.1:g.187130022_187130023delinsAG	GRCh37
NC_000004.10:g.187367016_187367017delinsAG	NCBI36
NG_007965.1:g.22349_22350delinsAG
NG_012095.2:g.4890_4891delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1094_1095delinsAG MANE Select	ENSP00000368079.4:p.Lys365=
ENST00000378802.4:c.1094_1095delinsAG	ENSP00000368079.4:p.Lys365=
ENST00000502665.1:n.329_330delinsAG
ENST00000507209.5:n.5792_5793delinsAG
ENST00000513354.5:n.184_185delinsAG
NM_207352.3:c.1094_1095delinsAG	NP_997235.3:p.Lys365=
XM_005262935.2:c.1094_1095delinsAG	XP_005262992.1:p.Lys365=
XM_006714184.2:c.698_699delinsAG	XP_006714247.1:p.Lys233=
XM_005262935.4:c.1094_1095delinsAG	XP_005262992.1:p.Lys365=
XM_017008037.1:c.698_699delinsAG	XP_016863526.1:p.Lys233=
NM_207352.4:c.1094_1095delinsAG MANE Select	NP_997235.3:p.Lys365=