Canonical Allele Identifier: CA1519888814

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736456664
• gnomAD v4: 4-186205076-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205079_186205081del , CM000666.2:g.186205079_186205081del	GRCh38
NC_000004.11:g.187126233_187126235del , CM000666.1:g.187126233_187126235del	GRCh37
NC_000004.10:g.187363227_187363229del	NCBI36
NG_007965.1:g.18560_18562del
NG_012095.2:g.1101_1103del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-121_988-119del MANE Select	ENSP00000368079.4:n.988-121_988-119del
ENST00000378802.4:c.988-121_988-119del	ENSP00000368079.4:n.988-121_988-119del
ENST00000502665.1:n.222+21_222+23del
ENST00000507209.5:n.5565_5567del
ENST00000513354.5:n.78-121_78-119del
NM_207352.3:c.988-121_988-119del	NP_997235.3:n.988-121_988-119del
XM_005262935.2:c.988-121_988-119del	XP_005262992.1:n.988-121_988-119del
XM_006714184.2:c.592-121_592-119del	XP_006714247.1:n.592-121_592-119del
XM_005262935.4:c.988-121_988-119del	XP_005262992.1:n.988-121_988-119del
XM_017008037.1:c.592-121_592-119del	XP_016863526.1:n.592-121_592-119del
NM_207352.4:c.988-121_988-119del MANE Select	NP_997235.3:n.988-121_988-119del