Canonical Allele Identifier: CA2672896209

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204795-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204796_186204797del , CM000666.2:g.186204796_186204797del	GRCh38
NC_000004.11:g.187125950_187125951del , CM000666.1:g.187125950_187125951del	GRCh37
NC_000004.10:g.187362944_187362945del	NCBI36
NG_007965.1:g.18277_18278del
NG_012095.2:g.818_819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-404_988-403del MANE Select	ENSP00000368079.4:n.988-404_988-403del
ENST00000378802.4:c.988-404_988-403del	ENSP00000368079.4:n.988-404_988-403del
ENST00000507209.5:n.5282_5283del
ENST00000513354.5:n.77+339_77+340del
NM_207352.3:c.988-404_988-403del	NP_997235.3:n.988-404_988-403del
XM_005262935.2:c.988-404_988-403del	XP_005262992.1:n.988-404_988-403del
XM_006714184.2:c.592-404_592-403del	XP_006714247.1:n.592-404_592-403del
XM_005262935.4:c.988-404_988-403del	XP_005262992.1:n.988-404_988-403del
XM_017008037.1:c.592-404_592-403del	XP_016863526.1:n.592-404_592-403del
NM_207352.4:c.988-404_988-403del MANE Select	NP_997235.3:n.988-404_988-403del