Canonical Allele Identifier: CA2672896216

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204796-CTGGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204797_186204801del , CM000666.2:g.186204797_186204801del	GRCh38
NC_000004.11:g.187125951_187125955del , CM000666.1:g.187125951_187125955del	GRCh37
NC_000004.10:g.187362945_187362949del	NCBI36
NG_007965.1:g.18278_18282del
NG_012095.2:g.819_823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-403_988-399del MANE Select	ENSP00000368079.4:n.988-403_988-399del
ENST00000378802.4:c.988-403_988-399del	ENSP00000368079.4:n.988-403_988-399del
ENST00000507209.5:n.5283_5287del
ENST00000513354.5:n.77+340_77+344del
NM_207352.3:c.988-403_988-399del	NP_997235.3:n.988-403_988-399del
XM_005262935.2:c.988-403_988-399del	XP_005262992.1:n.988-403_988-399del
XM_006714184.2:c.592-403_592-399del	XP_006714247.1:n.592-403_592-399del
XM_005262935.4:c.988-403_988-399del	XP_005262992.1:n.988-403_988-399del
XM_017008037.1:c.592-403_592-399del	XP_016863526.1:n.592-403_592-399del
NM_207352.4:c.988-403_988-399del MANE Select	NP_997235.3:n.988-403_988-399del