Canonical Allele Identifier: CA1002239135

Gene: CYP2J2

Linked Data

• gnomAD v3: 1-59919886-A-ACGGCG
• gnomAD v4: 1-59919886-A-ACGGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919886_59919887insCGGCG , CM000663.2:g.59919886_59919887insCGGCG	GRCh38
NC_000001.10:g.60385558_60385559insCGGCG , CM000663.1:g.60385558_60385559insCGGCG	GRCh37
NC_000001.9:g.60158146_60158147insCGGCG	NCBI36
NG_007931.1:g.11865_11866insCGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3787_211-3786insCGCCG MANE Select	ENSP00000360247.3:n.211-3787_211-3786insCGCCG
ENST00000468257.2:c.211-3787_211-3786insCGCCG	ENSP00000497807.1:n.211-3787_211-3786insCGCCG
ENST00000469406.6:c.227-3787_227-3786insCGCCG	ENSP00000497732.1:n.227-3787_227-3786insCGCCG
ENST00000371204.3:c.211-3787_211-3786insCGCCG	ENSP00000360247.3:n.211-3787_211-3786insCGCCG
ENST00000466095.5:n.226-3787_226-3786insCGCCG
ENST00000468257.1:n.236-3787_236-3786insCGCCG
ENST00000469406.5:n.226-3787_226-3786insCGCCG
NM_000775.2:c.211-3787_211-3786insCGCCG	NP_000766.2:n.211-3787_211-3786insCGCCG
XR_246240.2:n.238-3787_238-3786insCGCCG
XR_946558.1:n.238-3787_238-3786insCGCCG
NM_000775.3:c.211-3787_211-3786insCGCCG	NP_000766.2:n.211-3787_211-3786insCGCCG
NR_134981.1:n.263-3787_263-3786insCGCCG
NR_134982.1:n.263-3787_263-3786insCGCCG
NM_000775.4:c.211-3787_211-3786insCGCCG MANE Select	NP_000766.2:n.211-3787_211-3786insCGCCG
NR_134981.2:n.238-3787_238-3786insCGCCG
NR_134982.2:n.238-3787_238-3786insCGCCG