Canonical Allele Identifier: CA2672896237

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204804-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204805_186204806del , CM000666.2:g.186204805_186204806del	GRCh38
NC_000004.11:g.187125959_187125960del , CM000666.1:g.187125959_187125960del	GRCh37
NC_000004.10:g.187362953_187362954del	NCBI36
NG_007965.1:g.18286_18287del
NG_012095.2:g.827_828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-395_988-394del MANE Select	ENSP00000368079.4:n.988-395_988-394del
ENST00000378802.4:c.988-395_988-394del	ENSP00000368079.4:n.988-395_988-394del
ENST00000507209.5:n.5291_5292del
ENST00000513354.5:n.77+348_77+349del
NM_207352.3:c.988-395_988-394del	NP_997235.3:n.988-395_988-394del
XM_005262935.2:c.988-395_988-394del	XP_005262992.1:n.988-395_988-394del
XM_006714184.2:c.592-395_592-394del	XP_006714247.1:n.592-395_592-394del
XM_005262935.4:c.988-395_988-394del	XP_005262992.1:n.988-395_988-394del
XM_017008037.1:c.592-395_592-394del	XP_016863526.1:n.592-395_592-394del
NM_207352.4:c.988-395_988-394del MANE Select	NP_997235.3:n.988-395_988-394del