Canonical Allele Identifier: CA2324927938

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540734_15540735delinsTG , CM000681.2:g.15540734_15540735delinsTG	GRCh38
NC_000019.9:g.15651545_15651546delinsTG , CM000681.1:g.15651545_15651546delinsTG	GRCh37
NC_000019.8:g.15512545_15512546delinsTG	NCBI36
NG_007987.1:g.37210_37211delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+17_939+18delinsTG MANE Select	ENSP00000269703.1:n.939+17_939+18delinsTG
ENST00000269703.7:c.939+17_939+18delinsTG	ENSP00000269703.1:n.939+17_939+18delinsTG
ENST00000601005.2:c.939+17_939+18delinsTG	ENSP00000469866.1:n.939+17_939+18delinsTG
NM_173483.3:c.939+17_939+18delinsTG	NP_775754.2:n.939+17_939+18delinsTG
XM_011527692.1:c.939+17_939+18delinsTG	XP_011525994.1:n.939+17_939+18delinsTG
XM_011527693.1:c.939+17_939+18delinsTG	XP_011525995.1:n.939+17_939+18delinsTG
XM_011527692.2:c.939+17_939+18delinsTG	XP_011525994.1:n.939+17_939+18delinsTG
XM_011527693.2:c.939+17_939+18delinsTG	XP_011525995.1:n.939+17_939+18delinsTG
NM_173483.4:c.939+17_939+18delinsTG MANE Select	NP_775754.2:n.939+17_939+18delinsTG