Canonical Allele Identifier: CA2764868108

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205394_186205395insA , CM000666.2:g.186205394_186205395insA	GRCh38
NC_000004.11:g.187126548_187126549insA , CM000666.1:g.187126548_187126549insA	GRCh37
NC_000004.10:g.187363542_187363543insA	NCBI36
NG_007965.1:g.18875_18876insA
NG_012095.2:g.1416_1417insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+92_1090+93insA MANE Select	ENSP00000368079.4:n.1090+92_1090+93insA
ENST00000378802.4:c.1090+92_1090+93insA	ENSP00000368079.4:n.1090+92_1090+93insA
ENST00000502665.1:n.325+92_325+93insA
ENST00000507209.5:n.5788+92_5788+93insA
ENST00000513354.5:n.180+92_180+93insA
NM_207352.3:c.1090+92_1090+93insA	NP_997235.3:n.1090+92_1090+93insA
XM_005262935.2:c.1090+92_1090+93insA	XP_005262992.1:n.1090+92_1090+93insA
XM_006714184.2:c.694+92_694+93insA	XP_006714247.1:n.694+92_694+93insA
XM_005262935.4:c.1090+92_1090+93insA	XP_005262992.1:n.1090+92_1090+93insA
XM_017008037.1:c.694+92_694+93insA	XP_016863526.1:n.694+92_694+93insA
NM_207352.4:c.1090+92_1090+93insA MANE Select	NP_997235.3:n.1090+92_1090+93insA