Canonical Allele Identifier: CA2764867687

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204664_186204665del , CM000666.2:g.186204664_186204665del	GRCh38
NC_000004.11:g.187125818_187125819del , CM000666.1:g.187125818_187125819del	GRCh37
NC_000004.10:g.187362812_187362813del	NCBI36
NG_007965.1:g.18145_18146del
NG_012095.2:g.686_687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-536_988-535del MANE Select	ENSP00000368079.4:n.988-536_988-535del
ENST00000378802.4:c.988-536_988-535del	ENSP00000368079.4:n.988-536_988-535del
ENST00000507209.5:n.5150_5151del
ENST00000513354.5:n.77+207_77+208del
NM_207352.3:c.988-536_988-535del	NP_997235.3:n.988-536_988-535del
XM_005262935.2:c.988-536_988-535del	XP_005262992.1:n.988-536_988-535del
XM_006714184.2:c.592-536_592-535del	XP_006714247.1:n.592-536_592-535del
XM_005262935.4:c.988-536_988-535del	XP_005262992.1:n.988-536_988-535del
XM_017008037.1:c.592-536_592-535del	XP_016863526.1:n.592-536_592-535del
NM_207352.4:c.988-536_988-535del MANE Select	NP_997235.3:n.988-536_988-535del