Canonical Allele Identifier: CA2324927977

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540750_15540752delinsCCG , CM000681.2:g.15540750_15540752delinsCCG	GRCh38
NC_000019.9:g.15651561_15651563delinsCCG , CM000681.1:g.15651561_15651563delinsCCG	GRCh37
NC_000019.8:g.15512561_15512563delinsCCG	NCBI36
NG_007987.1:g.37226_37228delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+33_939+35delinsCCG MANE Select	ENSP00000269703.1:n.939+33_939+35delinsCCG
ENST00000269703.7:c.939+33_939+35delinsCCG	ENSP00000269703.1:n.939+33_939+35delinsCCG
ENST00000601005.2:c.939+33_939+35delinsCCG	ENSP00000469866.1:n.939+33_939+35delinsCCG
NM_173483.3:c.939+33_939+35delinsCCG	NP_775754.2:n.939+33_939+35delinsCCG
XM_011527692.1:c.939+33_939+35delinsCCG	XP_011525994.1:n.939+33_939+35delinsCCG
XM_011527693.1:c.939+33_939+35delinsCCG	XP_011525995.1:n.939+33_939+35delinsCCG
XM_011527692.2:c.939+33_939+35delinsCCG	XP_011525994.1:n.939+33_939+35delinsCCG
XM_011527693.2:c.939+33_939+35delinsCCG	XP_011525995.1:n.939+33_939+35delinsCCG
NM_173483.4:c.939+33_939+35delinsCCG MANE Select	NP_775754.2:n.939+33_939+35delinsCCG