Canonical Allele Identifier: CA2764867728

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204691_186204692insACA , CM000666.2:g.186204691_186204692insACA	GRCh38
NC_000004.11:g.187125845_187125846insACA , CM000666.1:g.187125845_187125846insACA	GRCh37
NC_000004.10:g.187362839_187362840insACA	NCBI36
NG_007965.1:g.18172_18173insACA
NG_012095.2:g.713_714insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-509_988-508insACA MANE Select	ENSP00000368079.4:n.988-509_988-508insACA
ENST00000378802.4:c.988-509_988-508insACA	ENSP00000368079.4:n.988-509_988-508insACA
ENST00000507209.5:n.5177_5178insACA
ENST00000513354.5:n.77+234_77+235insACA
NM_207352.3:c.988-509_988-508insACA	NP_997235.3:n.988-509_988-508insACA
XM_005262935.2:c.988-509_988-508insACA	XP_005262992.1:n.988-509_988-508insACA
XM_006714184.2:c.592-509_592-508insACA	XP_006714247.1:n.592-509_592-508insACA
XM_005262935.4:c.988-509_988-508insACA	XP_005262992.1:n.988-509_988-508insACA
XM_017008037.1:c.592-509_592-508insACA	XP_016863526.1:n.592-509_592-508insACA
NM_207352.4:c.988-509_988-508insACA MANE Select	NP_997235.3:n.988-509_988-508insACA