Canonical Allele Identifier: CA631956257

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1488932941
• gnomAD v2: 19-15654879-C-CAGG
• gnomAD v4: 19-15544068-C-CAGG
• MyVariant Identifiers: chr19:g.15654879_15654880insAGG (hg19) ; chr19:g.15544068_15544069insAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15544070_15544072dup , CM000681.2:g.15544070_15544072dup	GRCh38
NC_000019.9:g.15654881_15654883dup , CM000681.1:g.15654881_15654883dup	GRCh37
NC_000019.8:g.15515881_15515883dup	NCBI36
NG_007987.1:g.40546_40548dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269703.8:c.1006+33_1006+35dup MANE Select	ENSP00000269703.1:n.1006+33_1006+35dup
ENST00000269703.7:c.1006+33_1006+35dup	ENSP00000269703.1:n.1006+33_1006+35dup
ENST00000601005.2:c.1006+33_1006+35dup	ENSP00000469866.1:n.1006+33_1006+35dup
NM_173483.3:c.1006+33_1006+35dup	NP_775754.2:n.1006+33_1006+35dup
XM_011527692.1:c.1006+33_1006+35dup	XP_011525994.1:n.1006+33_1006+35dup
XM_011527693.1:c.1006+33_1006+35dup	XP_011525995.1:n.1006+33_1006+35dup
XM_011527692.2:c.1006+33_1006+35dup	XP_011525994.1:n.1006+33_1006+35dup
XM_011527693.2:c.1006+33_1006+35dup	XP_011525995.1:n.1006+33_1006+35dup
NM_173483.4:c.1006+33_1006+35dup MANE Select	NP_775754.2:n.1006+33_1006+35dup