Canonical Allele Identifier: CA2764868392

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199155_186199156insA , CM000666.2:g.186199155_186199156insA	GRCh38
NC_000004.11:g.187120309_187120310insA , CM000666.1:g.187120309_187120310insA	GRCh37
NC_000004.10:g.187357303_187357304insA	NCBI36
NG_007965.1:g.12636_12637insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.801+72_801+73insA MANE Select	ENSP00000368079.4:n.801+72_801+73insA
ENST00000378802.4:c.801+72_801+73insA	ENSP00000368079.4:n.801+72_801+73insA
ENST00000507209.5:n.1642+72_1642+73insA
NM_207352.3:c.801+72_801+73insA	NP_997235.3:n.801+72_801+73insA
XM_005262935.2:c.801+72_801+73insA	XP_005262992.1:n.801+72_801+73insA
XM_006714184.2:c.405+72_405+73insA	XP_006714247.1:n.405+72_405+73insA
XM_005262935.4:c.801+72_801+73insA	XP_005262992.1:n.801+72_801+73insA
XM_017008037.1:c.405+72_405+73insA	XP_016863526.1:n.405+72_405+73insA
NM_207352.4:c.801+72_801+73insA MANE Select	NP_997235.3:n.801+72_801+73insA