Canonical Allele Identifier: CA2764867759

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204704_186204705insACA , CM000666.2:g.186204704_186204705insACA	GRCh38
NC_000004.11:g.187125858_187125859insACA , CM000666.1:g.187125858_187125859insACA	GRCh37
NC_000004.10:g.187362852_187362853insACA	NCBI36
NG_007965.1:g.18185_18186insACA
NG_012095.2:g.726_727insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-496_988-495insACA MANE Select	ENSP00000368079.4:n.988-496_988-495insACA
ENST00000378802.4:c.988-496_988-495insACA	ENSP00000368079.4:n.988-496_988-495insACA
ENST00000507209.5:n.5190_5191insACA
ENST00000513354.5:n.77+247_77+248insACA
NM_207352.3:c.988-496_988-495insACA	NP_997235.3:n.988-496_988-495insACA
XM_005262935.2:c.988-496_988-495insACA	XP_005262992.1:n.988-496_988-495insACA
XM_006714184.2:c.592-496_592-495insACA	XP_006714247.1:n.592-496_592-495insACA
XM_005262935.4:c.988-496_988-495insACA	XP_005262992.1:n.988-496_988-495insACA
XM_017008037.1:c.592-496_592-495insACA	XP_016863526.1:n.592-496_592-495insACA
NM_207352.4:c.988-496_988-495insACA MANE Select	NP_997235.3:n.988-496_988-495insACA