Canonical Allele Identifier: CA2583108021

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540753-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540753_15540754insCT , CM000681.2:g.15540753_15540754insCT	GRCh38
NC_000019.9:g.15651564_15651565insCT , CM000681.1:g.15651564_15651565insCT	GRCh37
NC_000019.8:g.15512564_15512565insCT	NCBI36
NG_007987.1:g.37229_37230insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+36_939+37insCT MANE Select	ENSP00000269703.1:n.939+36_939+37insCT
ENST00000269703.7:c.939+36_939+37insCT	ENSP00000269703.1:n.939+36_939+37insCT
ENST00000601005.2:c.939+36_939+37insCT	ENSP00000469866.1:n.939+36_939+37insCT
NM_173483.3:c.939+36_939+37insCT	NP_775754.2:n.939+36_939+37insCT
XM_011527692.1:c.939+36_939+37insCT	XP_011525994.1:n.939+36_939+37insCT
XM_011527693.1:c.939+36_939+37insCT	XP_011525995.1:n.939+36_939+37insCT
XM_011527692.2:c.939+36_939+37insCT	XP_011525994.1:n.939+36_939+37insCT
XM_011527693.2:c.939+36_939+37insCT	XP_011525995.1:n.939+36_939+37insCT
NM_173483.4:c.939+36_939+37insCT MANE Select	NP_775754.2:n.939+36_939+37insCT