Canonical Allele Identifier: CA2571626782

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540745_15540746insGC , CM000681.2:g.15540745_15540746insGC	GRCh38
NC_000019.9:g.15651556_15651557insGC , CM000681.1:g.15651556_15651557insGC	GRCh37
NC_000019.8:g.15512556_15512557insGC	NCBI36
NG_007987.1:g.37221_37222insGC

Transcript Alleles

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