Canonical Allele Identifier: CA2324927941

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540737_15540739delinsAAT , CM000681.2:g.15540737_15540739delinsAAT	GRCh38
NC_000019.9:g.15651548_15651550delinsAAT , CM000681.1:g.15651548_15651550delinsAAT	GRCh37
NC_000019.8:g.15512548_15512550delinsAAT	NCBI36
NG_007987.1:g.37213_37215delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+20_939+22delinsAAT MANE Select	ENSP00000269703.1:n.939+20_939+22delinsAAT
ENST00000269703.7:c.939+20_939+22delinsAAT	ENSP00000269703.1:n.939+20_939+22delinsAAT
ENST00000601005.2:c.939+20_939+22delinsAAT	ENSP00000469866.1:n.939+20_939+22delinsAAT
NM_173483.3:c.939+20_939+22delinsAAT	NP_775754.2:n.939+20_939+22delinsAAT
XM_011527692.1:c.939+20_939+22delinsAAT	XP_011525994.1:n.939+20_939+22delinsAAT
XM_011527693.1:c.939+20_939+22delinsAAT	XP_011525995.1:n.939+20_939+22delinsAAT
XM_011527692.2:c.939+20_939+22delinsAAT	XP_011525994.1:n.939+20_939+22delinsAAT
XM_011527693.2:c.939+20_939+22delinsAAT	XP_011525995.1:n.939+20_939+22delinsAAT
NM_173483.4:c.939+20_939+22delinsAAT MANE Select	NP_775754.2:n.939+20_939+22delinsAAT