Canonical Allele Identifier: CA2764867211

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194693_186194695del , CM000666.2:g.186194693_186194695del	GRCh38
NC_000004.11:g.187115847_187115849del , CM000666.1:g.187115847_187115849del	GRCh37
NC_000004.10:g.187352841_187352843del	NCBI36
NG_007965.1:g.8174_8176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+81_327+83del MANE Select	ENSP00000368079.4:n.327+81_327+83del
ENST00000378802.4:c.327+81_327+83del	ENSP00000368079.4:n.327+81_327+83del
NM_207352.3:c.327+81_327+83del	NP_997235.3:n.327+81_327+83del
XM_005262935.2:c.327+81_327+83del	XP_005262992.1:n.327+81_327+83del
XM_006714184.2:c.17+81_17+83del	XP_006714247.1:n.17+81_17+83del
XM_005262935.4:c.327+81_327+83del	XP_005262992.1:n.327+81_327+83del
XM_017008037.1:c.17+81_17+83del	XP_016863526.1:n.17+81_17+83del
NM_207352.4:c.327+81_327+83del MANE Select	NP_997235.3:n.327+81_327+83del