Canonical Allele Identifier: CA2324927979

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540751_15540753delinsCGA , CM000681.2:g.15540751_15540753delinsCGA	GRCh38
NC_000019.9:g.15651562_15651564delinsCGA , CM000681.1:g.15651562_15651564delinsCGA	GRCh37
NC_000019.8:g.15512562_15512564delinsCGA	NCBI36
NG_007987.1:g.37227_37229delinsCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+34_939+36delinsCGA MANE Select	ENSP00000269703.1:n.939+34_939+36delinsCGA
ENST00000269703.7:c.939+34_939+36delinsCGA	ENSP00000269703.1:n.939+34_939+36delinsCGA
ENST00000601005.2:c.939+34_939+36delinsCGA	ENSP00000469866.1:n.939+34_939+36delinsCGA
NM_173483.3:c.939+34_939+36delinsCGA	NP_775754.2:n.939+34_939+36delinsCGA
XM_011527692.1:c.939+34_939+36delinsCGA	XP_011525994.1:n.939+34_939+36delinsCGA
XM_011527693.1:c.939+34_939+36delinsCGA	XP_011525995.1:n.939+34_939+36delinsCGA
XM_011527692.2:c.939+34_939+36delinsCGA	XP_011525994.1:n.939+34_939+36delinsCGA
XM_011527693.2:c.939+34_939+36delinsCGA	XP_011525995.1:n.939+34_939+36delinsCGA
NM_173483.4:c.939+34_939+36delinsCGA MANE Select	NP_775754.2:n.939+34_939+36delinsCGA