Canonical Allele Identifier: CA2583108023

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540755-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540755_15540756insA , CM000681.2:g.15540755_15540756insA	GRCh38
NC_000019.9:g.15651566_15651567insA , CM000681.1:g.15651566_15651567insA	GRCh37
NC_000019.8:g.15512566_15512567insA	NCBI36
NG_007987.1:g.37231_37232insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+38_939+39insA MANE Select	ENSP00000269703.1:n.939+38_939+39insA
ENST00000269703.7:c.939+38_939+39insA	ENSP00000269703.1:n.939+38_939+39insA
ENST00000601005.2:c.939+38_939+39insA	ENSP00000469866.1:n.939+38_939+39insA
NM_173483.3:c.939+38_939+39insA	NP_775754.2:n.939+38_939+39insA
XM_011527692.1:c.939+38_939+39insA	XP_011525994.1:n.939+38_939+39insA
XM_011527693.1:c.939+38_939+39insA	XP_011525995.1:n.939+38_939+39insA
XM_011527692.2:c.939+38_939+39insA	XP_011525994.1:n.939+38_939+39insA
XM_011527693.2:c.939+38_939+39insA	XP_011525995.1:n.939+38_939+39insA
NM_173483.4:c.939+38_939+39insA MANE Select	NP_775754.2:n.939+38_939+39insA