Canonical Allele Identifier: CA2764868370

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199138_186199139insAC , CM000666.2:g.186199138_186199139insAC	GRCh38
NC_000004.11:g.187120292_187120293insAC , CM000666.1:g.187120292_187120293insAC	GRCh37
NC_000004.10:g.187357286_187357287insAC	NCBI36
NG_007965.1:g.12619_12620insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+55_801+56insAC MANE Select	ENSP00000368079.4:n.801+55_801+56insAC
ENST00000378802.4:c.801+55_801+56insAC	ENSP00000368079.4:n.801+55_801+56insAC
ENST00000507209.5:n.1642+55_1642+56insAC
NM_207352.3:c.801+55_801+56insAC	NP_997235.3:n.801+55_801+56insAC
XM_005262935.2:c.801+55_801+56insAC	XP_005262992.1:n.801+55_801+56insAC
XM_006714184.2:c.405+55_405+56insAC	XP_006714247.1:n.405+55_405+56insAC
XM_005262935.4:c.801+55_801+56insAC	XP_005262992.1:n.801+55_801+56insAC
XM_017008037.1:c.405+55_405+56insAC	XP_016863526.1:n.405+55_405+56insAC
NM_207352.4:c.801+55_801+56insAC MANE Select	NP_997235.3:n.801+55_801+56insAC