Canonical Allele Identifier: CA2672897298

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197269-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197269_186197270insAA , CM000666.2:g.186197269_186197270insAA	GRCh38
NC_000004.11:g.187118423_187118424insAA , CM000666.1:g.187118423_187118424insAA	GRCh37
NC_000004.10:g.187355417_187355418insAA	NCBI36
NG_007965.1:g.10750_10751insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+139_604+140insAA MANE Select	ENSP00000368079.4:n.604+139_604+140insAA
ENST00000378802.4:c.604+139_604+140insAA	ENSP00000368079.4:n.604+139_604+140insAA
ENST00000507209.5:n.1182_1183insAA
NM_207352.3:c.604+139_604+140insAA	NP_997235.3:n.604+139_604+140insAA
XM_005262935.2:c.604+139_604+140insAA	XP_005262992.1:n.604+139_604+140insAA
XM_006714184.2:c.208+139_208+140insAA	XP_006714247.1:n.208+139_208+140insAA
XM_005262935.4:c.604+139_604+140insAA	XP_005262992.1:n.604+139_604+140insAA
XM_017008037.1:c.208+139_208+140insAA	XP_016863526.1:n.208+139_208+140insAA
NM_207352.4:c.604+139_604+140insAA MANE Select	NP_997235.3:n.604+139_604+140insAA