Canonical Allele Identifier: CA2764867194

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194681_186194682insAG , CM000666.2:g.186194681_186194682insAG	GRCh38
NC_000004.11:g.187115835_187115836insAG , CM000666.1:g.187115835_187115836insAG	GRCh37
NC_000004.10:g.187352829_187352830insAG	NCBI36
NG_007965.1:g.8162_8163insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+69_327+70insAG MANE Select	ENSP00000368079.4:n.327+69_327+70insAG
ENST00000378802.4:c.327+69_327+70insAG	ENSP00000368079.4:n.327+69_327+70insAG
NM_207352.3:c.327+69_327+70insAG	NP_997235.3:n.327+69_327+70insAG
XM_005262935.2:c.327+69_327+70insAG	XP_005262992.1:n.327+69_327+70insAG
XM_006714184.2:c.17+69_17+70insAG	XP_006714247.1:n.17+69_17+70insAG
XM_005262935.4:c.327+69_327+70insAG	XP_005262992.1:n.327+69_327+70insAG
XM_017008037.1:c.17+69_17+70insAG	XP_016863526.1:n.17+69_17+70insAG
NM_207352.4:c.327+69_327+70insAG MANE Select	NP_997235.3:n.327+69_327+70insAG