Canonical Allele Identifier: CA2324927952

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540741_15540743delinsGCT , CM000681.2:g.15540741_15540743delinsGCT	GRCh38
NC_000019.9:g.15651552_15651554delinsGCT , CM000681.1:g.15651552_15651554delinsGCT	GRCh37
NC_000019.8:g.15512552_15512554delinsGCT	NCBI36
NG_007987.1:g.37217_37219delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+24_939+26delinsGCT MANE Select	ENSP00000269703.1:n.939+24_939+26delinsGCT
ENST00000269703.7:c.939+24_939+26delinsGCT	ENSP00000269703.1:n.939+24_939+26delinsGCT
ENST00000601005.2:c.939+24_939+26delinsGCT	ENSP00000469866.1:n.939+24_939+26delinsGCT
NM_173483.3:c.939+24_939+26delinsGCT	NP_775754.2:n.939+24_939+26delinsGCT
XM_011527692.1:c.939+24_939+26delinsGCT	XP_011525994.1:n.939+24_939+26delinsGCT
XM_011527693.1:c.939+24_939+26delinsGCT	XP_011525995.1:n.939+24_939+26delinsGCT
XM_011527692.2:c.939+24_939+26delinsGCT	XP_011525994.1:n.939+24_939+26delinsGCT
XM_011527693.2:c.939+24_939+26delinsGCT	XP_011525995.1:n.939+24_939+26delinsGCT
NM_173483.4:c.939+24_939+26delinsGCT MANE Select	NP_775754.2:n.939+24_939+26delinsGCT