Canonical Allele Identifier: CA1519910566

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186191800_186191801delinsAC , CM000666.2:g.186191800_186191801delinsAC	GRCh38
NC_000004.11:g.187112954_187112955delinsAC , CM000666.1:g.187112954_187112955delinsAC	GRCh37
NC_000004.10:g.187349948_187349949delinsAC	NCBI36
NG_007965.1:g.5281_5282delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.-24_-23delinsAC MANE Select	ENSP00000368079.4:n.-24_-23delinsAC
ENST00000378802.4:c.-24_-23delinsAC	ENSP00000368079.4:n.-24_-23delinsAC
NM_207352.3:c.-24_-23delinsAC	NP_997235.3:n.-24_-23delinsAC
XM_005262935.2:c.-24_-23delinsAC	XP_005262992.1:n.-24_-23delinsAC
XM_005262935.4:c.-24_-23delinsAC	XP_005262992.1:n.-24_-23delinsAC
XM_017008037.1:c.-334_-333delinsAC	XP_016863526.1:n.-334_-333delinsAC
NM_207352.4:c.-24_-23delinsAC MANE Select	NP_997235.3:n.-24_-23delinsAC