Canonical Allele Identifier: CA632129601

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1360313794
• gnomAD v2: 19-15651555-G-GT
• gnomAD v4: 19-15540744-G-GT
• MyVariant Identifiers: chr19:g.15651555_15651556insT (hg19) ; chr19:g.15540744_15540745insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540744_15540745insT , CM000681.2:g.15540744_15540745insT	GRCh38
NC_000019.9:g.15651555_15651556insT , CM000681.1:g.15651555_15651556insT	GRCh37
NC_000019.8:g.15512555_15512556insT	NCBI36
NG_007987.1:g.37220_37221insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+27_939+28insT MANE Select	ENSP00000269703.1:n.939+27_939+28insT
ENST00000269703.7:c.939+27_939+28insT	ENSP00000269703.1:n.939+27_939+28insT
ENST00000601005.2:c.939+27_939+28insT	ENSP00000469866.1:n.939+27_939+28insT
NM_173483.3:c.939+27_939+28insT	NP_775754.2:n.939+27_939+28insT
XM_011527692.1:c.939+27_939+28insT	XP_011525994.1:n.939+27_939+28insT
XM_011527693.1:c.939+27_939+28insT	XP_011525995.1:n.939+27_939+28insT
XM_011527692.2:c.939+27_939+28insT	XP_011525994.1:n.939+27_939+28insT
XM_011527693.2:c.939+27_939+28insT	XP_011525995.1:n.939+27_939+28insT
NM_173483.4:c.939+27_939+28insT MANE Select	NP_775754.2:n.939+27_939+28insT