Canonical Allele Identifier: CA993929629

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971452427
• gnomAD v3: 19-15540752-G-GCT
• gnomAD v4: 19-15540752-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540752_15540753insCT , CM000681.2:g.15540752_15540753insCT	GRCh38
NC_000019.9:g.15651563_15651564insCT , CM000681.1:g.15651563_15651564insCT	GRCh37
NC_000019.8:g.15512563_15512564insCT	NCBI36
NG_007987.1:g.37228_37229insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+35_939+36insCT MANE Select	ENSP00000269703.1:n.939+35_939+36insCT
ENST00000269703.7:c.939+35_939+36insCT	ENSP00000269703.1:n.939+35_939+36insCT
ENST00000601005.2:c.939+35_939+36insCT	ENSP00000469866.1:n.939+35_939+36insCT
NM_173483.3:c.939+35_939+36insCT	NP_775754.2:n.939+35_939+36insCT
XM_011527692.1:c.939+35_939+36insCT	XP_011525994.1:n.939+35_939+36insCT
XM_011527693.1:c.939+35_939+36insCT	XP_011525995.1:n.939+35_939+36insCT
XM_011527692.2:c.939+35_939+36insCT	XP_011525994.1:n.939+35_939+36insCT
XM_011527693.2:c.939+35_939+36insCT	XP_011525995.1:n.939+35_939+36insCT
NM_173483.4:c.939+35_939+36insCT MANE Select	NP_775754.2:n.939+35_939+36insCT