Canonical Allele Identifier: CA1002239136

Gene: CYP2J2

Linked Data

• gnomAD v3: 1-59919887-A-ACCACC
• gnomAD v4: 1-59919887-A-ACCACC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919887_59919888insCCACC , CM000663.2:g.59919887_59919888insCCACC	GRCh38
NC_000001.10:g.60385559_60385560insCCACC , CM000663.1:g.60385559_60385560insCCACC	GRCh37
NC_000001.9:g.60158147_60158148insCCACC	NCBI36
NG_007931.1:g.11864_11865insGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3788_211-3787insGGTGG MANE Select	ENSP00000360247.3:n.211-3788_211-3787insGGTGG
ENST00000468257.2:c.211-3788_211-3787insGGTGG	ENSP00000497807.1:n.211-3788_211-3787insGGTGG
ENST00000469406.6:c.227-3788_227-3787insGGTGG	ENSP00000497732.1:n.227-3788_227-3787insGGTGG
ENST00000371204.3:c.211-3788_211-3787insGGTGG	ENSP00000360247.3:n.211-3788_211-3787insGGTGG
ENST00000466095.5:n.226-3788_226-3787insGGTGG
ENST00000468257.1:n.236-3788_236-3787insGGTGG
ENST00000469406.5:n.226-3788_226-3787insGGTGG
NM_000775.2:c.211-3788_211-3787insGGTGG	NP_000766.2:n.211-3788_211-3787insGGTGG
XR_246240.2:n.238-3788_238-3787insGGTGG
XR_946558.1:n.238-3788_238-3787insGGTGG
NM_000775.3:c.211-3788_211-3787insGGTGG	NP_000766.2:n.211-3788_211-3787insGGTGG
NR_134981.1:n.263-3788_263-3787insGGTGG
NR_134982.1:n.263-3788_263-3787insGGTGG
NM_000775.4:c.211-3788_211-3787insGGTGG MANE Select	NP_000766.2:n.211-3788_211-3787insGGTGG
NR_134981.2:n.238-3788_238-3787insGGTGG
NR_134982.2:n.238-3788_238-3787insGGTGG