Canonical Allele Identifier: CA2764867717

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204683_186204684insGT , CM000666.2:g.186204683_186204684insGT	GRCh38
NC_000004.11:g.187125837_187125838insGT , CM000666.1:g.187125837_187125838insGT	GRCh37
NC_000004.10:g.187362831_187362832insGT	NCBI36
NG_007965.1:g.18164_18165insGT
NG_012095.2:g.705_706insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-517_988-516insGT MANE Select	ENSP00000368079.4:n.988-517_988-516insGT
ENST00000378802.4:c.988-517_988-516insGT	ENSP00000368079.4:n.988-517_988-516insGT
ENST00000507209.5:n.5169_5170insGT
ENST00000513354.5:n.77+226_77+227insGT
NM_207352.3:c.988-517_988-516insGT	NP_997235.3:n.988-517_988-516insGT
XM_005262935.2:c.988-517_988-516insGT	XP_005262992.1:n.988-517_988-516insGT
XM_006714184.2:c.592-517_592-516insGT	XP_006714247.1:n.592-517_592-516insGT
XM_005262935.4:c.988-517_988-516insGT	XP_005262992.1:n.988-517_988-516insGT
XM_017008037.1:c.592-517_592-516insGT	XP_016863526.1:n.592-517_592-516insGT
NM_207352.4:c.988-517_988-516insGT MANE Select	NP_997235.3:n.988-517_988-516insGT