Canonical Allele Identifier: CA2583108022

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540753-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540753_15540754insC , CM000681.2:g.15540753_15540754insC	GRCh38
NC_000019.9:g.15651564_15651565insC , CM000681.1:g.15651564_15651565insC	GRCh37
NC_000019.8:g.15512564_15512565insC	NCBI36
NG_007987.1:g.37229_37230insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+36_939+37insC MANE Select	ENSP00000269703.1:n.939+36_939+37insC
ENST00000269703.7:c.939+36_939+37insC	ENSP00000269703.1:n.939+36_939+37insC
ENST00000601005.2:c.939+36_939+37insC	ENSP00000469866.1:n.939+36_939+37insC
NM_173483.3:c.939+36_939+37insC	NP_775754.2:n.939+36_939+37insC
XM_011527692.1:c.939+36_939+37insC	XP_011525994.1:n.939+36_939+37insC
XM_011527693.1:c.939+36_939+37insC	XP_011525995.1:n.939+36_939+37insC
XM_011527692.2:c.939+36_939+37insC	XP_011525994.1:n.939+36_939+37insC
XM_011527693.2:c.939+36_939+37insC	XP_011525995.1:n.939+36_939+37insC
NM_173483.4:c.939+36_939+37insC MANE Select	NP_775754.2:n.939+36_939+37insC