Canonical Allele Identifier: CA2764867621

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204624_186204625insACA , CM000666.2:g.186204624_186204625insACA	GRCh38
NC_000004.11:g.187125778_187125779insACA , CM000666.1:g.187125778_187125779insACA	GRCh37
NC_000004.10:g.187362772_187362773insACA	NCBI36
NG_007965.1:g.18105_18106insACA
NG_012095.2:g.646_647insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-576_988-575insACA MANE Select	ENSP00000368079.4:n.988-576_988-575insACA
ENST00000378802.4:c.988-576_988-575insACA	ENSP00000368079.4:n.988-576_988-575insACA
ENST00000507209.5:n.5110_5111insACA
ENST00000513354.5:n.77+167_77+168insACA
NM_207352.3:c.988-576_988-575insACA	NP_997235.3:n.988-576_988-575insACA
XM_005262935.2:c.988-576_988-575insACA	XP_005262992.1:n.988-576_988-575insACA
XM_006714184.2:c.592-576_592-575insACA	XP_006714247.1:n.592-576_592-575insACA
XM_005262935.4:c.988-576_988-575insACA	XP_005262992.1:n.988-576_988-575insACA
XM_017008037.1:c.592-576_592-575insACA	XP_016863526.1:n.592-576_592-575insACA
NM_207352.4:c.988-576_988-575insACA MANE Select	NP_997235.3:n.988-576_988-575insACA