Canonical Allele Identifier: CA1519888928

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205198_186205199delinsAG , CM000666.2:g.186205198_186205199delinsAG	GRCh38
NC_000004.11:g.187126352_187126353delinsAG , CM000666.1:g.187126352_187126353delinsAG	GRCh37
NC_000004.10:g.187363346_187363347delinsAG	NCBI36
NG_007965.1:g.18679_18680delinsAG
NG_012095.2:g.1220_1221delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-2_988-1delinsAG MANE Select	ENSP00000368079.4:n.988-2_988-1delinsAG
ENST00000378802.4:c.988-2_988-1delinsAG	ENSP00000368079.4:n.988-2_988-1delinsAG
ENST00000502665.1:n.223-2_223-1delinsAG
ENST00000507209.5:n.5684_5685delinsAG
ENST00000513354.5:n.78-2_78-1delinsAG
NM_207352.3:c.988-2_988-1delinsAG	NP_997235.3:n.988-2_988-1delinsAG
XM_005262935.2:c.988-2_988-1delinsAG	XP_005262992.1:n.988-2_988-1delinsAG
XM_006714184.2:c.592-2_592-1delinsAG	XP_006714247.1:n.592-2_592-1delinsAG
XM_005262935.4:c.988-2_988-1delinsAG	XP_005262992.1:n.988-2_988-1delinsAG
XM_017008037.1:c.592-2_592-1delinsAG	XP_016863526.1:n.592-2_592-1delinsAG
NM_207352.4:c.988-2_988-1delinsAG MANE Select	NP_997235.3:n.988-2_988-1delinsAG