Canonical Allele Identifier: CA2764867679

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204659_186204660insAC , CM000666.2:g.186204659_186204660insAC	GRCh38
NC_000004.11:g.187125813_187125814insAC , CM000666.1:g.187125813_187125814insAC	GRCh37
NC_000004.10:g.187362807_187362808insAC	NCBI36
NG_007965.1:g.18140_18141insAC
NG_012095.2:g.681_682insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-541_988-540insAC MANE Select	ENSP00000368079.4:n.988-541_988-540insAC
ENST00000378802.4:c.988-541_988-540insAC	ENSP00000368079.4:n.988-541_988-540insAC
ENST00000507209.5:n.5145_5146insAC
ENST00000513354.5:n.77+202_77+203insAC
NM_207352.3:c.988-541_988-540insAC	NP_997235.3:n.988-541_988-540insAC
XM_005262935.2:c.988-541_988-540insAC	XP_005262992.1:n.988-541_988-540insAC
XM_006714184.2:c.592-541_592-540insAC	XP_006714247.1:n.592-541_592-540insAC
XM_005262935.4:c.988-541_988-540insAC	XP_005262992.1:n.988-541_988-540insAC
XM_017008037.1:c.592-541_592-540insAC	XP_016863526.1:n.592-541_592-540insAC
NM_207352.4:c.988-541_988-540insAC MANE Select	NP_997235.3:n.988-541_988-540insAC