Canonical Allele Identifier: CA2672896816

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205086-TTGCAGTCACAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205095_186205105del , CM000666.2:g.186205095_186205105del	GRCh38
NC_000004.11:g.187126249_187126259del , CM000666.1:g.187126249_187126259del	GRCh37
NC_000004.10:g.187363243_187363253del	NCBI36
NG_007965.1:g.18576_18586del
NG_012095.2:g.1117_1127del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-105_988-95del MANE Select	ENSP00000368079.4:n.988-105_988-95del
ENST00000378802.4:c.988-105_988-95del	ENSP00000368079.4:n.988-105_988-95del
ENST00000502665.1:n.222+37_222+47del
ENST00000507209.5:n.5581_5591del
ENST00000513354.5:n.78-105_78-95del
NM_207352.3:c.988-105_988-95del	NP_997235.3:n.988-105_988-95del
XM_005262935.2:c.988-105_988-95del	XP_005262992.1:n.988-105_988-95del
XM_006714184.2:c.592-105_592-95del	XP_006714247.1:n.592-105_592-95del
XM_005262935.4:c.988-105_988-95del	XP_005262992.1:n.988-105_988-95del
XM_017008037.1:c.592-105_592-95del	XP_016863526.1:n.592-105_592-95del
NM_207352.4:c.988-105_988-95del MANE Select	NP_997235.3:n.988-105_988-95del