Canonical Allele Identifier: CA2542460471

Gene: CYP2J2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59920024_59920026del , CM000663.2:g.59920024_59920026del	GRCh38
NC_000001.10:g.60385696_60385698del , CM000663.1:g.60385696_60385698del	GRCh37
NC_000001.9:g.60158284_60158286del	NCBI36
NG_007931.1:g.11729_11731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3923_211-3921del MANE Select	ENSP00000360247.3:n.211-3923_211-3921del
ENST00000468257.2:c.211-3923_211-3921del	ENSP00000497807.1:n.211-3923_211-3921del
ENST00000469406.6:c.227-3923_227-3921del	ENSP00000497732.1:n.227-3923_227-3921del
ENST00000371204.3:c.211-3923_211-3921del	ENSP00000360247.3:n.211-3923_211-3921del
ENST00000466095.5:n.226-3923_226-3921del
ENST00000468257.1:n.236-3923_236-3921del
ENST00000469406.5:n.226-3923_226-3921del
NM_000775.2:c.211-3923_211-3921del	NP_000766.2:n.211-3923_211-3921del
XR_246240.2:n.238-3923_238-3921del
XR_946558.1:n.238-3923_238-3921del
NM_000775.3:c.211-3923_211-3921del	NP_000766.2:n.211-3923_211-3921del
NR_134981.1:n.263-3923_263-3921del
NR_134982.1:n.263-3923_263-3921del
NM_000775.4:c.211-3923_211-3921del MANE Select	NP_000766.2:n.211-3923_211-3921del
NR_134981.2:n.238-3923_238-3921del
NR_134982.2:n.238-3923_238-3921del