Canonical Allele Identifier: CA2764867201

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194686_186194687del , CM000666.2:g.186194686_186194687del	GRCh38
NC_000004.11:g.187115840_187115841del , CM000666.1:g.187115840_187115841del	GRCh37
NC_000004.10:g.187352834_187352835del	NCBI36
NG_007965.1:g.8167_8168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+74_327+75del MANE Select	ENSP00000368079.4:n.327+74_327+75del
ENST00000378802.4:c.327+74_327+75del	ENSP00000368079.4:n.327+74_327+75del
NM_207352.3:c.327+74_327+75del	NP_997235.3:n.327+74_327+75del
XM_005262935.2:c.327+74_327+75del	XP_005262992.1:n.327+74_327+75del
XM_006714184.2:c.17+74_17+75del	XP_006714247.1:n.17+74_17+75del
XM_005262935.4:c.327+74_327+75del	XP_005262992.1:n.327+74_327+75del
XM_017008037.1:c.17+74_17+75del	XP_016863526.1:n.17+74_17+75del
NM_207352.4:c.327+74_327+75del MANE Select	NP_997235.3:n.327+74_327+75del