Canonical Allele Identifier: CA2324927984

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540753_15540757delinsAGGGC , CM000681.2:g.15540753_15540757delinsAGGGC	GRCh38
NC_000019.9:g.15651564_15651568delinsAGGGC , CM000681.1:g.15651564_15651568delinsAGGGC	GRCh37
NC_000019.8:g.15512564_15512568delinsAGGGC	NCBI36
NG_007987.1:g.37229_37233delinsAGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+36_939+40delinsAGGGC MANE Select	ENSP00000269703.1:n.939+36_939+40delinsAGGGC
ENST00000269703.7:c.939+36_939+40delinsAGGGC	ENSP00000269703.1:n.939+36_939+40delinsAGGGC
ENST00000601005.2:c.939+36_939+40delinsAGGGC	ENSP00000469866.1:n.939+36_939+40delinsAGGGC
NM_173483.3:c.939+36_939+40delinsAGGGC	NP_775754.2:n.939+36_939+40delinsAGGGC
XM_011527692.1:c.939+36_939+40delinsAGGGC	XP_011525994.1:n.939+36_939+40delinsAGGGC
XM_011527693.1:c.939+36_939+40delinsAGGGC	XP_011525995.1:n.939+36_939+40delinsAGGGC
XM_011527692.2:c.939+36_939+40delinsAGGGC	XP_011525994.1:n.939+36_939+40delinsAGGGC
XM_011527693.2:c.939+36_939+40delinsAGGGC	XP_011525995.1:n.939+36_939+40delinsAGGGC
NM_173483.4:c.939+36_939+40delinsAGGGC MANE Select	NP_775754.2:n.939+36_939+40delinsAGGGC