Canonical Allele Identifier: CA2583108012

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540745-G-GGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540745_15540746insGGC , CM000681.2:g.15540745_15540746insGGC	GRCh38
NC_000019.9:g.15651556_15651557insGGC , CM000681.1:g.15651556_15651557insGGC	GRCh37
NC_000019.8:g.15512556_15512557insGGC	NCBI36
NG_007987.1:g.37221_37222insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+28_939+29insGGC MANE Select	ENSP00000269703.1:n.939+28_939+29insGGC
ENST00000269703.7:c.939+28_939+29insGGC	ENSP00000269703.1:n.939+28_939+29insGGC
ENST00000601005.2:c.939+28_939+29insGGC	ENSP00000469866.1:n.939+28_939+29insGGC
NM_173483.3:c.939+28_939+29insGGC	NP_775754.2:n.939+28_939+29insGGC
XM_011527692.1:c.939+28_939+29insGGC	XP_011525994.1:n.939+28_939+29insGGC
XM_011527693.1:c.939+28_939+29insGGC	XP_011525995.1:n.939+28_939+29insGGC
XM_011527692.2:c.939+28_939+29insGGC	XP_011525994.1:n.939+28_939+29insGGC
XM_011527693.2:c.939+28_939+29insGGC	XP_011525995.1:n.939+28_939+29insGGC
NM_173483.4:c.939+28_939+29insGGC MANE Select	NP_775754.2:n.939+28_939+29insGGC