Canonical Allele Identifier: CA2672895347

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186194657-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194661_186194662del , CM000666.2:g.186194661_186194662del	GRCh38
NC_000004.11:g.187115815_187115816del , CM000666.1:g.187115815_187115816del	GRCh37
NC_000004.10:g.187352809_187352810del	NCBI36
NG_007965.1:g.8142_8143del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.327+49_327+50del MANE Select	ENSP00000368079.4:n.327+49_327+50del
ENST00000378802.4:c.327+49_327+50del	ENSP00000368079.4:n.327+49_327+50del
NM_207352.3:c.327+49_327+50del	NP_997235.3:n.327+49_327+50del
XM_005262935.2:c.327+49_327+50del	XP_005262992.1:n.327+49_327+50del
XM_006714184.2:c.17+49_17+50del	XP_006714247.1:n.17+49_17+50del
XM_005262935.4:c.327+49_327+50del	XP_005262992.1:n.327+49_327+50del
XM_017008037.1:c.17+49_17+50del	XP_016863526.1:n.17+49_17+50del
NM_207352.4:c.327+49_327+50del MANE Select	NP_997235.3:n.327+49_327+50del