Canonical Allele Identifier: CA2764867629

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204630_186204634del , CM000666.2:g.186204630_186204634del	GRCh38
NC_000004.11:g.187125784_187125788del , CM000666.1:g.187125784_187125788del	GRCh37
NC_000004.10:g.187362778_187362782del	NCBI36
NG_007965.1:g.18111_18115del
NG_012095.2:g.652_656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-570_988-566del MANE Select	ENSP00000368079.4:n.988-570_988-566del
ENST00000378802.4:c.988-570_988-566del	ENSP00000368079.4:n.988-570_988-566del
ENST00000507209.5:n.5116_5120del
ENST00000513354.5:n.77+173_77+177del
NM_207352.3:c.988-570_988-566del	NP_997235.3:n.988-570_988-566del
XM_005262935.2:c.988-570_988-566del	XP_005262992.1:n.988-570_988-566del
XM_006714184.2:c.592-570_592-566del	XP_006714247.1:n.592-570_592-566del
XM_005262935.4:c.988-570_988-566del	XP_005262992.1:n.988-570_988-566del
XM_017008037.1:c.592-570_592-566del	XP_016863526.1:n.592-570_592-566del
NM_207352.4:c.988-570_988-566del MANE Select	NP_997235.3:n.988-570_988-566del