Canonical Allele Identifier: CA404536575

Gene: CYP4F22

Linked Data

• gnomAD v2: 19-15651560-CCCGAG-C
• MyVariant Identifiers: chr19:g.15651561_15651565del (hg19) ; chr19:g.15540750_15540754del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540750_15540754del , CM000681.2:g.15540750_15540754del	GRCh38
NC_000019.9:g.15651561_15651565del , CM000681.1:g.15651561_15651565del	GRCh37
NC_000019.8:g.15512561_15512565del	NCBI36
NG_007987.1:g.37226_37230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+33_939+37del MANE Select	ENSP00000269703.1:n.939+33_939+37del
ENST00000269703.7:c.939+33_939+37del	ENSP00000269703.1:n.939+33_939+37del
ENST00000601005.2:c.939+33_939+37del	ENSP00000469866.1:n.939+33_939+37del
NM_173483.3:c.939+33_939+37del	NP_775754.2:n.939+33_939+37del
XM_011527692.1:c.939+33_939+37del	XP_011525994.1:n.939+33_939+37del
XM_011527693.1:c.939+33_939+37del	XP_011525995.1:n.939+33_939+37del
XM_011527692.2:c.939+33_939+37del	XP_011525994.1:n.939+33_939+37del
XM_011527693.2:c.939+33_939+37del	XP_011525995.1:n.939+33_939+37del
NM_173483.4:c.939+33_939+37del MANE Select	NP_775754.2:n.939+33_939+37del