Canonical Allele Identifier: CA993929615

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971452055
• gnomAD v3: 19-15540748-TCCC-T
• gnomAD v4: 19-15540748-TCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540749_15540751del , CM000681.2:g.15540749_15540751del	GRCh38
NC_000019.9:g.15651560_15651562del , CM000681.1:g.15651560_15651562del	GRCh37
NC_000019.8:g.15512560_15512562del	NCBI36
NG_007987.1:g.37225_37227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+32_939+34del MANE Select	ENSP00000269703.1:n.939+32_939+34del
ENST00000269703.7:c.939+32_939+34del	ENSP00000269703.1:n.939+32_939+34del
ENST00000601005.2:c.939+32_939+34del	ENSP00000469866.1:n.939+32_939+34del
NM_173483.3:c.939+32_939+34del	NP_775754.2:n.939+32_939+34del
XM_011527692.1:c.939+32_939+34del	XP_011525994.1:n.939+32_939+34del
XM_011527693.1:c.939+32_939+34del	XP_011525995.1:n.939+32_939+34del
XM_011527692.2:c.939+32_939+34del	XP_011525994.1:n.939+32_939+34del
XM_011527693.2:c.939+32_939+34del	XP_011525995.1:n.939+32_939+34del
NM_173483.4:c.939+32_939+34del MANE Select	NP_775754.2:n.939+32_939+34del