Canonical Allele Identifier: CA2764867631

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204631_186204632insACA , CM000666.2:g.186204631_186204632insACA	GRCh38
NC_000004.11:g.187125785_187125786insACA , CM000666.1:g.187125785_187125786insACA	GRCh37
NC_000004.10:g.187362779_187362780insACA	NCBI36
NG_007965.1:g.18112_18113insACA
NG_012095.2:g.653_654insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-569_988-568insACA MANE Select	ENSP00000368079.4:n.988-569_988-568insACA
ENST00000378802.4:c.988-569_988-568insACA	ENSP00000368079.4:n.988-569_988-568insACA
ENST00000507209.5:n.5117_5118insACA
ENST00000513354.5:n.77+174_77+175insACA
NM_207352.3:c.988-569_988-568insACA	NP_997235.3:n.988-569_988-568insACA
XM_005262935.2:c.988-569_988-568insACA	XP_005262992.1:n.988-569_988-568insACA
XM_006714184.2:c.592-569_592-568insACA	XP_006714247.1:n.592-569_592-568insACA
XM_005262935.4:c.988-569_988-568insACA	XP_005262992.1:n.988-569_988-568insACA
XM_017008037.1:c.592-569_592-568insACA	XP_016863526.1:n.592-569_592-568insACA
NM_207352.4:c.988-569_988-568insACA MANE Select	NP_997235.3:n.988-569_988-568insACA