Canonical Allele Identifier: CA1519891302

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208895_186208896delinsAC , CM000666.2:g.186208895_186208896delinsAC	GRCh38
NC_000004.11:g.187130049_187130050delinsAC , CM000666.1:g.187130049_187130050delinsAC	GRCh37
NC_000004.10:g.187367043_187367044delinsAC	NCBI36
NG_007965.1:g.22376_22377delinsAC
NG_012095.2:g.4917_4918delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1121_1122delinsAC MANE Select	ENSP00000368079.4:p.Asp374=
ENST00000378802.4:c.1121_1122delinsAC	ENSP00000368079.4:p.Asp374=
ENST00000502665.1:n.356_357delinsAC
ENST00000507209.5:n.5819_5820delinsAC
ENST00000513354.5:n.211_212delinsAC
NM_207352.3:c.1121_1122delinsAC	NP_997235.3:p.Asp374=
XM_005262935.2:c.1121_1122delinsAC	XP_005262992.1:p.Asp374=
XM_006714184.2:c.725_726delinsAC	XP_006714247.1:p.Asp242=
XM_005262935.4:c.1121_1122delinsAC	XP_005262992.1:p.Asp374=
XM_017008037.1:c.725_726delinsAC	XP_016863526.1:p.Asp242=
NM_207352.4:c.1121_1122delinsAC MANE Select	NP_997235.3:p.Asp374=