Canonical Allele Identifier: CA2583108008

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540739-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540739_15540740insG , CM000681.2:g.15540739_15540740insG	GRCh38
NC_000019.9:g.15651550_15651551insG , CM000681.1:g.15651550_15651551insG	GRCh37
NC_000019.8:g.15512550_15512551insG	NCBI36
NG_007987.1:g.37215_37216insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+22_939+23insG MANE Select	ENSP00000269703.1:n.939+22_939+23insG
ENST00000269703.7:c.939+22_939+23insG	ENSP00000269703.1:n.939+22_939+23insG
ENST00000601005.2:c.939+22_939+23insG	ENSP00000469866.1:n.939+22_939+23insG
NM_173483.3:c.939+22_939+23insG	NP_775754.2:n.939+22_939+23insG
XM_011527692.1:c.939+22_939+23insG	XP_011525994.1:n.939+22_939+23insG
XM_011527693.1:c.939+22_939+23insG	XP_011525995.1:n.939+22_939+23insG
XM_011527692.2:c.939+22_939+23insG	XP_011525994.1:n.939+22_939+23insG
XM_011527693.2:c.939+22_939+23insG	XP_011525995.1:n.939+22_939+23insG
NM_173483.4:c.939+22_939+23insG MANE Select	NP_775754.2:n.939+22_939+23insG