Canonical Allele Identifier: CA1002239119

Gene: CYP2J2

Linked Data

• gnomAD v3: 1-59919874-T-TTTA
• gnomAD v4: 1-59919874-T-TTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919874_59919875insTTA , CM000663.2:g.59919874_59919875insTTA	GRCh38
NC_000001.10:g.60385546_60385547insTTA , CM000663.1:g.60385546_60385547insTTA	GRCh37
NC_000001.9:g.60158134_60158135insTTA	NCBI36
NG_007931.1:g.11877_11878insTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3775_211-3774insTAA MANE Select	ENSP00000360247.3:n.211-3775_211-3774insTAA
ENST00000468257.2:c.211-3775_211-3774insTAA	ENSP00000497807.1:n.211-3775_211-3774insTAA
ENST00000469406.6:c.227-3775_227-3774insTAA	ENSP00000497732.1:n.227-3775_227-3774insTAA
ENST00000371204.3:c.211-3775_211-3774insTAA	ENSP00000360247.3:n.211-3775_211-3774insTAA
ENST00000466095.5:n.226-3775_226-3774insTAA
ENST00000468257.1:n.236-3775_236-3774insTAA
ENST00000469406.5:n.226-3775_226-3774insTAA
NM_000775.2:c.211-3775_211-3774insTAA	NP_000766.2:n.211-3775_211-3774insTAA
XR_246240.2:n.238-3775_238-3774insTAA
XR_946558.1:n.238-3775_238-3774insTAA
NM_000775.3:c.211-3775_211-3774insTAA	NP_000766.2:n.211-3775_211-3774insTAA
NR_134981.1:n.263-3775_263-3774insTAA
NR_134982.1:n.263-3775_263-3774insTAA
NM_000775.4:c.211-3775_211-3774insTAA MANE Select	NP_000766.2:n.211-3775_211-3774insTAA
NR_134981.2:n.238-3775_238-3774insTAA
NR_134982.2:n.238-3775_238-3774insTAA