Canonical Allele Identifier: CA9269770

Gene: CYP4F22

Linked Data

• dbSNP Id: rs777399765
• ExAC: 19:15651564 AGGGC / A
• gnomAD v4: 19-15540753-AGGGC-A
• MyVariant Identifiers: chr19:g.15651565_15651568del (hg19) ; chr19:g.15540754_15540757del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540754_15540757del , CM000681.2:g.15540754_15540757del	GRCh38
NC_000019.9:g.15651565_15651568del , CM000681.1:g.15651565_15651568del	GRCh37
NC_000019.8:g.15512565_15512568del	NCBI36
NG_007987.1:g.37230_37233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+37_939+40del MANE Select	ENSP00000269703.1:n.939+37_939+40del
ENST00000269703.7:c.939+37_939+40del	ENSP00000269703.1:n.939+37_939+40del
ENST00000601005.2:c.939+37_939+40del	ENSP00000469866.1:n.939+37_939+40del
NM_173483.3:c.939+37_939+40del	NP_775754.2:n.939+37_939+40del
XM_011527692.1:c.939+37_939+40del	XP_011525994.1:n.939+37_939+40del
XM_011527693.1:c.939+37_939+40del	XP_011525995.1:n.939+37_939+40del
XM_011527692.2:c.939+37_939+40del	XP_011525994.1:n.939+37_939+40del
XM_011527693.2:c.939+37_939+40del	XP_011525995.1:n.939+37_939+40del
NM_173483.4:c.939+37_939+40del MANE Select	NP_775754.2:n.939+37_939+40del