Canonical Allele Identifier: CA2764867171

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194674_186194675insAGTT , CM000666.2:g.186194674_186194675insAGTT	GRCh38
NC_000004.11:g.187115828_187115829insAGTT , CM000666.1:g.187115828_187115829insAGTT	GRCh37
NC_000004.10:g.187352822_187352823insAGTT	NCBI36
NG_007965.1:g.8155_8156insAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+62_327+63insAGTT MANE Select	ENSP00000368079.4:n.327+62_327+63insAGTT
ENST00000378802.4:c.327+62_327+63insAGTT	ENSP00000368079.4:n.327+62_327+63insAGTT
NM_207352.3:c.327+62_327+63insAGTT	NP_997235.3:n.327+62_327+63insAGTT
XM_005262935.2:c.327+62_327+63insAGTT	XP_005262992.1:n.327+62_327+63insAGTT
XM_006714184.2:c.17+62_17+63insAGTT	XP_006714247.1:n.17+62_17+63insAGTT
XM_005262935.4:c.327+62_327+63insAGTT	XP_005262992.1:n.327+62_327+63insAGTT
XM_017008037.1:c.17+62_17+63insAGTT	XP_016863526.1:n.17+62_17+63insAGTT
NM_207352.4:c.327+62_327+63insAGTT MANE Select	NP_997235.3:n.327+62_327+63insAGTT