Canonical Allele Identifier: CA2324927945

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540738_15540739delinsAT , CM000681.2:g.15540738_15540739delinsAT	GRCh38
NC_000019.9:g.15651549_15651550delinsAT , CM000681.1:g.15651549_15651550delinsAT	GRCh37
NC_000019.8:g.15512549_15512550delinsAT	NCBI36
NG_007987.1:g.37214_37215delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+21_939+22delinsAT MANE Select	ENSP00000269703.1:n.939+21_939+22delinsAT
ENST00000269703.7:c.939+21_939+22delinsAT	ENSP00000269703.1:n.939+21_939+22delinsAT
ENST00000601005.2:c.939+21_939+22delinsAT	ENSP00000469866.1:n.939+21_939+22delinsAT
NM_173483.3:c.939+21_939+22delinsAT	NP_775754.2:n.939+21_939+22delinsAT
XM_011527692.1:c.939+21_939+22delinsAT	XP_011525994.1:n.939+21_939+22delinsAT
XM_011527693.1:c.939+21_939+22delinsAT	XP_011525995.1:n.939+21_939+22delinsAT
XM_011527692.2:c.939+21_939+22delinsAT	XP_011525994.1:n.939+21_939+22delinsAT
XM_011527693.2:c.939+21_939+22delinsAT	XP_011525995.1:n.939+21_939+22delinsAT
NM_173483.4:c.939+21_939+22delinsAT MANE Select	NP_775754.2:n.939+21_939+22delinsAT