Canonical Allele Identifier: CA1519914832

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194424_186194425delinsGA , CM000666.2:g.186194424_186194425delinsGA	GRCh38
NC_000004.11:g.187115578_187115579delinsGA , CM000666.1:g.187115578_187115579delinsGA	GRCh37
NC_000004.10:g.187352572_187352573delinsGA	NCBI36
NG_007965.1:g.7905_7906delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.215-76_215-75delinsGA MANE Select	ENSP00000368079.4:n.215-76_215-75delinsGA
ENST00000378802.4:c.215-76_215-75delinsGA	ENSP00000368079.4:n.215-76_215-75delinsGA
NM_207352.3:c.215-76_215-75delinsGA	NP_997235.3:n.215-76_215-75delinsGA
XM_005262935.2:c.215-76_215-75delinsGA	XP_005262992.1:n.215-76_215-75delinsGA
XM_005262935.4:c.215-76_215-75delinsGA	XP_005262992.1:n.215-76_215-75delinsGA
XM_017008037.1:c.-96-76_-96-75delinsGA	XP_016863526.1:n.-96-76_-96-75delinsGA
NM_207352.4:c.215-76_215-75delinsGA MANE Select	NP_997235.3:n.215-76_215-75delinsGA