Canonical Allele Identifier: CA2764867718

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204684_186204686del , CM000666.2:g.186204684_186204686del	GRCh38
NC_000004.11:g.187125838_187125840del , CM000666.1:g.187125838_187125840del	GRCh37
NC_000004.10:g.187362832_187362834del	NCBI36
NG_007965.1:g.18165_18167del
NG_012095.2:g.706_708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-516_988-514del MANE Select	ENSP00000368079.4:n.988-516_988-514del
ENST00000378802.4:c.988-516_988-514del	ENSP00000368079.4:n.988-516_988-514del
ENST00000507209.5:n.5170_5172del
ENST00000513354.5:n.77+227_77+229del
NM_207352.3:c.988-516_988-514del	NP_997235.3:n.988-516_988-514del
XM_005262935.2:c.988-516_988-514del	XP_005262992.1:n.988-516_988-514del
XM_006714184.2:c.592-516_592-514del	XP_006714247.1:n.592-516_592-514del
XM_005262935.4:c.988-516_988-514del	XP_005262992.1:n.988-516_988-514del
XM_017008037.1:c.592-516_592-514del	XP_016863526.1:n.592-516_592-514del
NM_207352.4:c.988-516_988-514del MANE Select	NP_997235.3:n.988-516_988-514del