Canonical Allele Identifier: CA632129585

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1568361462
• gnomAD v2: 19-15651493-AC-A
• gnomAD v4: 19-15540682-AC-A
• MyVariant Identifiers: chr19:g.15651494del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540684del , CM000681.2:g.15540684del	GRCh38
NC_000019.9:g.15651495del , CM000681.1:g.15651495del	GRCh37
NC_000019.8:g.15512495del	NCBI36
NG_007987.1:g.37160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.906del MANE Select	ENSP00000269703.1:p.Leu303TrpfsTer?
ENST00000269703.7:c.906del	ENSP00000269703.1:p.Leu303TrpfsTer?
ENST00000601005.2:c.906del	ENSP00000469866.1:p.Leu303TrpfsTer?
NM_173483.3:c.906del	NP_775754.2:p.Leu303TrpfsTer?
XM_011527692.1:c.906del	XP_011525994.1:p.Leu303TrpfsTer?
XM_011527693.1:c.906del	XP_011525995.1:p.Leu303TrpfsTer?
XM_011527692.2:c.906del	XP_011525994.1:p.Leu303TrpfsTer?
XM_011527693.2:c.906del	XP_011525995.1:p.Leu303TrpfsTer?
NM_173483.4:c.906del MANE Select	NP_775754.2:p.Leu303TrpfsTer?