Canonical Allele Identifier: CA920067575

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1555729252

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540737_15540755del , CM000681.2:g.15540737_15540755del	GRCh38
NC_000019.9:g.15651548_15651566del , CM000681.1:g.15651548_15651566del	GRCh37
NC_000019.8:g.15512548_15512566del	NCBI36
NG_007987.1:g.37213_37231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+20_939+38del MANE Select	ENSP00000269703.1:n.939+20_939+38del
ENST00000269703.7:c.939+20_939+38del	ENSP00000269703.1:n.939+20_939+38del
ENST00000601005.2:c.939+20_939+38del	ENSP00000469866.1:n.939+20_939+38del
NM_173483.3:c.939+20_939+38del	NP_775754.2:n.939+20_939+38del
XM_011527692.1:c.939+20_939+38del	XP_011525994.1:n.939+20_939+38del
XM_011527693.1:c.939+20_939+38del	XP_011525995.1:n.939+20_939+38del
XM_011527692.2:c.939+20_939+38del	XP_011525994.1:n.939+20_939+38del
XM_011527693.2:c.939+20_939+38del	XP_011525995.1:n.939+20_939+38del
NM_173483.4:c.939+20_939+38del MANE Select	NP_775754.2:n.939+20_939+38del