Canonical Allele Identifier: CA2764868285

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205520_186205521insA , CM000666.2:g.186205520_186205521insA	GRCh38
NC_000004.11:g.187126674_187126675insA , CM000666.1:g.187126674_187126675insA	GRCh37
NC_000004.10:g.187363668_187363669insA	NCBI36
NG_007965.1:g.19001_19002insA
NG_012095.2:g.1542_1543insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+218_1090+219insA MANE Select	ENSP00000368079.4:n.1090+218_1090+219insA
ENST00000378802.4:c.1090+218_1090+219insA	ENSP00000368079.4:n.1090+218_1090+219insA
ENST00000502665.1:n.325+218_325+219insA
ENST00000507209.5:n.5788+218_5788+219insA
ENST00000513354.5:n.180+218_180+219insA
NM_207352.3:c.1090+218_1090+219insA	NP_997235.3:n.1090+218_1090+219insA
XM_005262935.2:c.1090+218_1090+219insA	XP_005262992.1:n.1090+218_1090+219insA
XM_006714184.2:c.694+218_694+219insA	XP_006714247.1:n.694+218_694+219insA
XM_005262935.4:c.1090+218_1090+219insA	XP_005262992.1:n.1090+218_1090+219insA
XM_017008037.1:c.694+218_694+219insA	XP_016863526.1:n.694+218_694+219insA
NM_207352.4:c.1090+218_1090+219insA MANE Select	NP_997235.3:n.1090+218_1090+219insA