Canonical Allele Identifier: CA2583108016

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540751-C-CTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540751_15540752insTGT , CM000681.2:g.15540751_15540752insTGT	GRCh38
NC_000019.9:g.15651562_15651563insTGT , CM000681.1:g.15651562_15651563insTGT	GRCh37
NC_000019.8:g.15512562_15512563insTGT	NCBI36
NG_007987.1:g.37227_37228insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+34_939+35insTGT MANE Select	ENSP00000269703.1:n.939+34_939+35insTGT
ENST00000269703.7:c.939+34_939+35insTGT	ENSP00000269703.1:n.939+34_939+35insTGT
ENST00000601005.2:c.939+34_939+35insTGT	ENSP00000469866.1:n.939+34_939+35insTGT
NM_173483.3:c.939+34_939+35insTGT	NP_775754.2:n.939+34_939+35insTGT
XM_011527692.1:c.939+34_939+35insTGT	XP_011525994.1:n.939+34_939+35insTGT
XM_011527693.1:c.939+34_939+35insTGT	XP_011525995.1:n.939+34_939+35insTGT
XM_011527692.2:c.939+34_939+35insTGT	XP_011525994.1:n.939+34_939+35insTGT
XM_011527693.2:c.939+34_939+35insTGT	XP_011525995.1:n.939+34_939+35insTGT
NM_173483.4:c.939+34_939+35insTGT MANE Select	NP_775754.2:n.939+34_939+35insTGT