Canonical Allele Identifier: CA2764868254

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205469_186205470insACA , CM000666.2:g.186205469_186205470insACA	GRCh38
NC_000004.11:g.187126623_187126624insACA , CM000666.1:g.187126623_187126624insACA	GRCh37
NC_000004.10:g.187363617_187363618insACA	NCBI36
NG_007965.1:g.18950_18951insACA
NG_012095.2:g.1491_1492insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+167_1090+168insACA MANE Select	ENSP00000368079.4:n.1090+167_1090+168insACA
ENST00000378802.4:c.1090+167_1090+168insACA	ENSP00000368079.4:n.1090+167_1090+168insACA
ENST00000502665.1:n.325+167_325+168insACA
ENST00000507209.5:n.5788+167_5788+168insACA
ENST00000513354.5:n.180+167_180+168insACA
NM_207352.3:c.1090+167_1090+168insACA	NP_997235.3:n.1090+167_1090+168insACA
XM_005262935.2:c.1090+167_1090+168insACA	XP_005262992.1:n.1090+167_1090+168insACA
XM_006714184.2:c.694+167_694+168insACA	XP_006714247.1:n.694+167_694+168insACA
XM_005262935.4:c.1090+167_1090+168insACA	XP_005262992.1:n.1090+167_1090+168insACA
XM_017008037.1:c.694+167_694+168insACA	XP_016863526.1:n.694+167_694+168insACA
NM_207352.4:c.1090+167_1090+168insACA MANE Select	NP_997235.3:n.1090+167_1090+168insACA