Canonical Allele Identifier: CA2764867696

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204666_186204667insTC , CM000666.2:g.186204666_186204667insTC	GRCh38
NC_000004.11:g.187125820_187125821insTC , CM000666.1:g.187125820_187125821insTC	GRCh37
NC_000004.10:g.187362814_187362815insTC	NCBI36
NG_007965.1:g.18147_18148insTC
NG_012095.2:g.688_689insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-534_988-533insTC MANE Select	ENSP00000368079.4:n.988-534_988-533insTC
ENST00000378802.4:c.988-534_988-533insTC	ENSP00000368079.4:n.988-534_988-533insTC
ENST00000507209.5:n.5152_5153insTC
ENST00000513354.5:n.77+209_77+210insTC
NM_207352.3:c.988-534_988-533insTC	NP_997235.3:n.988-534_988-533insTC
XM_005262935.2:c.988-534_988-533insTC	XP_005262992.1:n.988-534_988-533insTC
XM_006714184.2:c.592-534_592-533insTC	XP_006714247.1:n.592-534_592-533insTC
XM_005262935.4:c.988-534_988-533insTC	XP_005262992.1:n.988-534_988-533insTC
XM_017008037.1:c.592-534_592-533insTC	XP_016863526.1:n.592-534_592-533insTC
NM_207352.4:c.988-534_988-533insTC MANE Select	NP_997235.3:n.988-534_988-533insTC