Canonical Allele Identifier: CA9269760

Gene: CYP4F22

Linked Data

• ClinVar Variation Id: 1262638
• ClinVar RCV Id: RCV001669871
• dbSNP Id: rs374797305
• ExAC: 19:15651556 G / GAGC
• gnomAD v2: 19-15651556-G-GAGC
• gnomAD v3: 19-15540745-G-GAGC
• gnomAD v4: 19-15540745-G-GAGC
• MyVariant Identifiers: chr19:g.15651556_15651557insAGC (hg19) ; chr19:g.15540745_15540746insAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540745_15540746insAGC , CM000681.2:g.15540745_15540746insAGC	GRCh38
NC_000019.9:g.15651556_15651557insAGC , CM000681.1:g.15651556_15651557insAGC	GRCh37
NC_000019.8:g.15512556_15512557insAGC	NCBI36
NG_007987.1:g.37221_37222insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+28_939+29insAGC MANE Select	ENSP00000269703.1:n.939+28_939+29insAGC
ENST00000269703.7:c.939+28_939+29insAGC	ENSP00000269703.1:n.939+28_939+29insAGC
ENST00000601005.2:c.939+28_939+29insAGC	ENSP00000469866.1:n.939+28_939+29insAGC
NM_173483.3:c.939+28_939+29insAGC	NP_775754.2:n.939+28_939+29insAGC
XM_011527692.1:c.939+28_939+29insAGC	XP_011525994.1:n.939+28_939+29insAGC
XM_011527693.1:c.939+28_939+29insAGC	XP_011525995.1:n.939+28_939+29insAGC
XM_011527692.2:c.939+28_939+29insAGC	XP_011525994.1:n.939+28_939+29insAGC
XM_011527693.2:c.939+28_939+29insAGC	XP_011525995.1:n.939+28_939+29insAGC
NM_173483.4:c.939+28_939+29insAGC MANE Select	NP_775754.2:n.939+28_939+29insAGC