Canonical Allele Identifier: CA2324927652

Gene: CYP4F22

Linked Data

• dbSNP Id: rs537649124

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540731_15540733del , CM000681.2:g.15540731_15540733del	GRCh38
NC_000019.9:g.15651542_15651544del , CM000681.1:g.15651542_15651544del	GRCh37
NC_000019.8:g.15512542_15512544del	NCBI36
NG_007987.1:g.37207_37209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+14_939+16del MANE Select	ENSP00000269703.1:n.939+14_939+16del
ENST00000269703.7:c.939+14_939+16del	ENSP00000269703.1:n.939+14_939+16del
ENST00000601005.2:c.939+14_939+16del	ENSP00000469866.1:n.939+14_939+16del
NM_173483.3:c.939+14_939+16del	NP_775754.2:n.939+14_939+16del
XM_011527692.1:c.939+14_939+16del	XP_011525994.1:n.939+14_939+16del
XM_011527693.1:c.939+14_939+16del	XP_011525995.1:n.939+14_939+16del
XM_011527692.2:c.939+14_939+16del	XP_011525994.1:n.939+14_939+16del
XM_011527693.2:c.939+14_939+16del	XP_011525995.1:n.939+14_939+16del
NM_173483.4:c.939+14_939+16del MANE Select	NP_775754.2:n.939+14_939+16del