Canonical Allele Identifier: CA2764868380

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199145_186199146insAGAT , CM000666.2:g.186199145_186199146insAGAT	GRCh38
NC_000004.11:g.187120299_187120300insAGAT , CM000666.1:g.187120299_187120300insAGAT	GRCh37
NC_000004.10:g.187357293_187357294insAGAT	NCBI36
NG_007965.1:g.12626_12627insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+62_801+63insAGAT MANE Select	ENSP00000368079.4:n.801+62_801+63insAGAT
ENST00000378802.4:c.801+62_801+63insAGAT	ENSP00000368079.4:n.801+62_801+63insAGAT
ENST00000507209.5:n.1642+62_1642+63insAGAT
NM_207352.3:c.801+62_801+63insAGAT	NP_997235.3:n.801+62_801+63insAGAT
XM_005262935.2:c.801+62_801+63insAGAT	XP_005262992.1:n.801+62_801+63insAGAT
XM_006714184.2:c.405+62_405+63insAGAT	XP_006714247.1:n.405+62_405+63insAGAT
XM_005262935.4:c.801+62_801+63insAGAT	XP_005262992.1:n.801+62_801+63insAGAT
XM_017008037.1:c.405+62_405+63insAGAT	XP_016863526.1:n.405+62_405+63insAGAT
NM_207352.4:c.801+62_801+63insAGAT MANE Select	NP_997235.3:n.801+62_801+63insAGAT