Canonical Allele Identifier: CA920067580

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1568361566

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540742_15540745delinsGAGC , CM000681.2:g.15540742_15540745delinsGAGC	GRCh38
NC_000019.9:g.15651553_15651556delinsGAGC , CM000681.1:g.15651553_15651556delinsGAGC	GRCh37
NC_000019.8:g.15512553_15512556delinsGAGC	NCBI36
NG_007987.1:g.37218_37221delinsGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+25_939+28delinsGAGC MANE Select	ENSP00000269703.1:n.939+25_939+28delinsGAGC
ENST00000269703.7:c.939+25_939+28delinsGAGC	ENSP00000269703.1:n.939+25_939+28delinsGAGC
ENST00000601005.2:c.939+25_939+28delinsGAGC	ENSP00000469866.1:n.939+25_939+28delinsGAGC
NM_173483.3:c.939+25_939+28delinsGAGC	NP_775754.2:n.939+25_939+28delinsGAGC
XM_011527692.1:c.939+25_939+28delinsGAGC	XP_011525994.1:n.939+25_939+28delinsGAGC
XM_011527693.1:c.939+25_939+28delinsGAGC	XP_011525995.1:n.939+25_939+28delinsGAGC
XM_011527692.2:c.939+25_939+28delinsGAGC	XP_011525994.1:n.939+25_939+28delinsGAGC
XM_011527693.2:c.939+25_939+28delinsGAGC	XP_011525995.1:n.939+25_939+28delinsGAGC
NM_173483.4:c.939+25_939+28delinsGAGC MANE Select	NP_775754.2:n.939+25_939+28delinsGAGC