Canonical Allele Identifier: CA305826647

Gene: CYP4F22

Linked Data

• dbSNP Id: rs748408004
• gnomAD v2: 19-15651549-ATT-A
• gnomAD v4: 19-15540738-ATT-A
• MyVariant Identifiers: chr19:g.15651550_15651551del (hg19) ; chr19:g.15540739_15540740del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540739_15540740del , CM000681.2:g.15540739_15540740del	GRCh38
NC_000019.9:g.15651550_15651551del , CM000681.1:g.15651550_15651551del	GRCh37
NC_000019.8:g.15512550_15512551del	NCBI36
NG_007987.1:g.37215_37216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+22_939+23del MANE Select	ENSP00000269703.1:n.939+22_939+23del
ENST00000269703.7:c.939+22_939+23del	ENSP00000269703.1:n.939+22_939+23del
ENST00000601005.2:c.939+22_939+23del	ENSP00000469866.1:n.939+22_939+23del
NM_173483.3:c.939+22_939+23del	NP_775754.2:n.939+22_939+23del
XM_011527692.1:c.939+22_939+23del	XP_011525994.1:n.939+22_939+23del
XM_011527693.1:c.939+22_939+23del	XP_011525995.1:n.939+22_939+23del
XM_011527692.2:c.939+22_939+23del	XP_011525994.1:n.939+22_939+23del
XM_011527693.2:c.939+22_939+23del	XP_011525995.1:n.939+22_939+23del
NM_173483.4:c.939+22_939+23del MANE Select	NP_775754.2:n.939+22_939+23del