Canonical Allele Identifier: CA2324927946

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971451049

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540738_15540743del , CM000681.2:g.15540738_15540743del	GRCh38
NC_000019.9:g.15651549_15651554del , CM000681.1:g.15651549_15651554del	GRCh37
NC_000019.8:g.15512549_15512554del	NCBI36
NG_007987.1:g.37214_37219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+21_939+26del MANE Select	ENSP00000269703.1:n.939+21_939+26del
ENST00000269703.7:c.939+21_939+26del	ENSP00000269703.1:n.939+21_939+26del
ENST00000601005.2:c.939+21_939+26del	ENSP00000469866.1:n.939+21_939+26del
NM_173483.3:c.939+21_939+26del	NP_775754.2:n.939+21_939+26del
XM_011527692.1:c.939+21_939+26del	XP_011525994.1:n.939+21_939+26del
XM_011527693.1:c.939+21_939+26del	XP_011525995.1:n.939+21_939+26del
XM_011527692.2:c.939+21_939+26del	XP_011525994.1:n.939+21_939+26del
XM_011527693.2:c.939+21_939+26del	XP_011525995.1:n.939+21_939+26del
NM_173483.4:c.939+21_939+26del MANE Select	NP_775754.2:n.939+21_939+26del