Canonical Allele Identifier: CA9269757

Gene: CYP4F22

Linked Data

• dbSNP Id: rs763303179
• ExAC: 19:15651552 G / GGAGCC
• gnomAD v2: 19-15651552-G-GGAGCC
• gnomAD v3: 19-15540741-G-GGAGCC
• gnomAD v4: 19-15540741-G-GGAGCC
• MyVariant Identifiers: chr19:g.15651552_15651553insGAGCC (hg19) ; chr19:g.15540741_15540742insGAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540741_15540742insGAGCC , CM000681.2:g.15540741_15540742insGAGCC	GRCh38
NC_000019.9:g.15651552_15651553insGAGCC , CM000681.1:g.15651552_15651553insGAGCC	GRCh37
NC_000019.8:g.15512552_15512553insGAGCC	NCBI36
NG_007987.1:g.37217_37218insGAGCC

Transcript Alleles

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