Canonical Allele Identifier: CA9269756

Gene: CYP4F22

Linked Data

• dbSNP Id: rs763303179
• ExAC: 19:15651552 G / GGGTAGAGCC
• gnomAD v2: 19-15651552-G-GGGTAGAGCC
• gnomAD v3: 19-15540741-G-GGGTAGAGCC
• gnomAD v4: 19-15540741-G-GGGTAGAGCC
• MyVariant Identifiers: chr19:g.15651552_15651553insGGTAGAGCC (hg19) ; chr19:g.15540741_15540742insGGTAGAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540741_15540742insGGTAGAGCC , CM000681.2:g.15540741_15540742insGGTAGAGCC	GRCh38
NC_000019.9:g.15651552_15651553insGGTAGAGCC , CM000681.1:g.15651552_15651553insGGTAGAGCC	GRCh37
NC_000019.8:g.15512552_15512553insGGTAGAGCC	NCBI36
NG_007987.1:g.37217_37218insGGTAGAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+24_939+25insGGTAGAGCC MANE Select	ENSP00000269703.1:n.939+24_939+25insGGTAGAGCC
ENST00000269703.7:c.939+24_939+25insGGTAGAGCC	ENSP00000269703.1:n.939+24_939+25insGGTAGAGCC
ENST00000601005.2:c.939+24_939+25insGGTAGAGCC	ENSP00000469866.1:n.939+24_939+25insGGTAGAGCC
NM_173483.3:c.939+24_939+25insGGTAGAGCC	NP_775754.2:n.939+24_939+25insGGTAGAGCC
XM_011527692.1:c.939+24_939+25insGGTAGAGCC	XP_011525994.1:n.939+24_939+25insGGTAGAGCC
XM_011527693.1:c.939+24_939+25insGGTAGAGCC	XP_011525995.1:n.939+24_939+25insGGTAGAGCC
XM_011527692.2:c.939+24_939+25insGGTAGAGCC	XP_011525994.1:n.939+24_939+25insGGTAGAGCC
XM_011527693.2:c.939+24_939+25insGGTAGAGCC	XP_011525995.1:n.939+24_939+25insGGTAGAGCC
NM_173483.4:c.939+24_939+25insGGTAGAGCC MANE Select	NP_775754.2:n.939+24_939+25insGGTAGAGCC