Canonical Allele Identifier: CA2672896308

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204836-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204836_186204837insA , CM000666.2:g.186204836_186204837insA	GRCh38
NC_000004.11:g.187125990_187125991insA , CM000666.1:g.187125990_187125991insA	GRCh37
NC_000004.10:g.187362984_187362985insA	NCBI36
NG_007965.1:g.18317_18318insA
NG_012095.2:g.858_859insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-364_988-363insA MANE Select	ENSP00000368079.4:n.988-364_988-363insA
ENST00000378802.4:c.988-364_988-363insA	ENSP00000368079.4:n.988-364_988-363insA
ENST00000502665.1:n.1-1_1insA
ENST00000507209.5:n.5322_5323insA
ENST00000513354.5:n.78-364_78-363insA
NM_207352.3:c.988-364_988-363insA	NP_997235.3:n.988-364_988-363insA
XM_005262935.2:c.988-364_988-363insA	XP_005262992.1:n.988-364_988-363insA
XM_006714184.2:c.592-364_592-363insA	XP_006714247.1:n.592-364_592-363insA
XM_005262935.4:c.988-364_988-363insA	XP_005262992.1:n.988-364_988-363insA
XM_017008037.1:c.592-364_592-363insA	XP_016863526.1:n.592-364_592-363insA
NM_207352.4:c.988-364_988-363insA MANE Select	NP_997235.3:n.988-364_988-363insA