Canonical Allele Identifier: CA2324927958

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540743_15540744delinsTG , CM000681.2:g.15540743_15540744delinsTG	GRCh38
NC_000019.9:g.15651554_15651555delinsTG , CM000681.1:g.15651554_15651555delinsTG	GRCh37
NC_000019.8:g.15512554_15512555delinsTG	NCBI36
NG_007987.1:g.37219_37220delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+26_939+27delinsTG MANE Select	ENSP00000269703.1:n.939+26_939+27delinsTG
ENST00000269703.7:c.939+26_939+27delinsTG	ENSP00000269703.1:n.939+26_939+27delinsTG
ENST00000601005.2:c.939+26_939+27delinsTG	ENSP00000469866.1:n.939+26_939+27delinsTG
NM_173483.3:c.939+26_939+27delinsTG	NP_775754.2:n.939+26_939+27delinsTG
XM_011527692.1:c.939+26_939+27delinsTG	XP_011525994.1:n.939+26_939+27delinsTG
XM_011527693.1:c.939+26_939+27delinsTG	XP_011525995.1:n.939+26_939+27delinsTG
XM_011527692.2:c.939+26_939+27delinsTG	XP_011525994.1:n.939+26_939+27delinsTG
XM_011527693.2:c.939+26_939+27delinsTG	XP_011525995.1:n.939+26_939+27delinsTG
NM_173483.4:c.939+26_939+27delinsTG MANE Select	NP_775754.2:n.939+26_939+27delinsTG