Canonical Allele Identifier: CA2324927955

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540742_15540743delinsCT , CM000681.2:g.15540742_15540743delinsCT	GRCh38
NC_000019.9:g.15651553_15651554delinsCT , CM000681.1:g.15651553_15651554delinsCT	GRCh37
NC_000019.8:g.15512553_15512554delinsCT	NCBI36
NG_007987.1:g.37218_37219delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+25_939+26delinsCT MANE Select	ENSP00000269703.1:n.939+25_939+26delinsCT
ENST00000269703.7:c.939+25_939+26delinsCT	ENSP00000269703.1:n.939+25_939+26delinsCT
ENST00000601005.2:c.939+25_939+26delinsCT	ENSP00000469866.1:n.939+25_939+26delinsCT
NM_173483.3:c.939+25_939+26delinsCT	NP_775754.2:n.939+25_939+26delinsCT
XM_011527692.1:c.939+25_939+26delinsCT	XP_011525994.1:n.939+25_939+26delinsCT
XM_011527693.1:c.939+25_939+26delinsCT	XP_011525995.1:n.939+25_939+26delinsCT
XM_011527692.2:c.939+25_939+26delinsCT	XP_011525994.1:n.939+25_939+26delinsCT
XM_011527693.2:c.939+25_939+26delinsCT	XP_011525995.1:n.939+25_939+26delinsCT
NM_173483.4:c.939+25_939+26delinsCT MANE Select	NP_775754.2:n.939+25_939+26delinsCT