Canonical Allele Identifier: CA2583108006

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540729-C-CTCCACCCTCCAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540729_15540730insTCCACCCTCCAGGG , CM000681.2:g.15540729_15540730insTCCACCCTCCAGGG	GRCh38
NC_000019.9:g.15651540_15651541insTCCACCCTCCAGGG , CM000681.1:g.15651540_15651541insTCCACCCTCCAGGG	GRCh37
NC_000019.8:g.15512540_15512541insTCCACCCTCCAGGG	NCBI36
NG_007987.1:g.37205_37206insTCCACCCTCCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+12_939+13insTCCACCCTCCAGGG MANE Select	ENSP00000269703.1:n.939+12_939+13insTCCACCCTCCAGGG
ENST00000269703.7:c.939+12_939+13insTCCACCCTCCAGGG	ENSP00000269703.1:n.939+12_939+13insTCCACCCTCCAGGG
ENST00000601005.2:c.939+12_939+13insTCCACCCTCCAGGG	ENSP00000469866.1:n.939+12_939+13insTCCACCCTCCAGGG
NM_173483.3:c.939+12_939+13insTCCACCCTCCAGGG	NP_775754.2:n.939+12_939+13insTCCACCCTCCAGGG
XM_011527692.1:c.939+12_939+13insTCCACCCTCCAGGG	XP_011525994.1:n.939+12_939+13insTCCACCCTCCAGGG
XM_011527693.1:c.939+12_939+13insTCCACCCTCCAGGG	XP_011525995.1:n.939+12_939+13insTCCACCCTCCAGGG
XM_011527692.2:c.939+12_939+13insTCCACCCTCCAGGG	XP_011525994.1:n.939+12_939+13insTCCACCCTCCAGGG
XM_011527693.2:c.939+12_939+13insTCCACCCTCCAGGG	XP_011525995.1:n.939+12_939+13insTCCACCCTCCAGGG
NM_173483.4:c.939+12_939+13insTCCACCCTCCAGGG MANE Select	NP_775754.2:n.939+12_939+13insTCCACCCTCCAGGG