Canonical Allele Identifier: CA9269771

Gene: CYP4F22

Linked Data

• dbSNP Id: rs746600784
• ExAC: 19:15651564 A / AT
• gnomAD v4: 19-15540753-A-AT
• MyVariant Identifiers: chr19:g.15651564_15651565insT (hg19) ; chr19:g.15651565_15651568delinsTGGGC (hg19) ; chr19:g.15540753_15540754insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540753_15540754insT , CM000681.2:g.15540753_15540754insT	GRCh38
NC_000019.9:g.15651564_15651565insT , CM000681.1:g.15651564_15651565insT	GRCh37
NC_000019.8:g.15512564_15512565insT	NCBI36
NG_007987.1:g.37229_37230insT

Transcript Alleles

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