Canonical Allele Identifier: CA2764867632

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204631_186204632insACTC , CM000666.2:g.186204631_186204632insACTC	GRCh38
NC_000004.11:g.187125785_187125786insACTC , CM000666.1:g.187125785_187125786insACTC	GRCh37
NC_000004.10:g.187362779_187362780insACTC	NCBI36
NG_007965.1:g.18112_18113insACTC
NG_012095.2:g.653_654insACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-569_988-568insACTC MANE Select	ENSP00000368079.4:n.988-569_988-568insACTC
ENST00000378802.4:c.988-569_988-568insACTC	ENSP00000368079.4:n.988-569_988-568insACTC
ENST00000507209.5:n.5117_5118insACTC
ENST00000513354.5:n.77+174_77+175insACTC
NM_207352.3:c.988-569_988-568insACTC	NP_997235.3:n.988-569_988-568insACTC
XM_005262935.2:c.988-569_988-568insACTC	XP_005262992.1:n.988-569_988-568insACTC
XM_006714184.2:c.592-569_592-568insACTC	XP_006714247.1:n.592-569_592-568insACTC
XM_005262935.4:c.988-569_988-568insACTC	XP_005262992.1:n.988-569_988-568insACTC
XM_017008037.1:c.592-569_592-568insACTC	XP_016863526.1:n.592-569_592-568insACTC
NM_207352.4:c.988-569_988-568insACTC MANE Select	NP_997235.3:n.988-569_988-568insACTC