Canonical Allele Identifier: CA2583108018

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540752-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540752_15540753insCC , CM000681.2:g.15540752_15540753insCC	GRCh38
NC_000019.9:g.15651563_15651564insCC , CM000681.1:g.15651563_15651564insCC	GRCh37
NC_000019.8:g.15512563_15512564insCC	NCBI36
NG_007987.1:g.37228_37229insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+35_939+36insCC MANE Select	ENSP00000269703.1:n.939+35_939+36insCC
ENST00000269703.7:c.939+35_939+36insCC	ENSP00000269703.1:n.939+35_939+36insCC
ENST00000601005.2:c.939+35_939+36insCC	ENSP00000469866.1:n.939+35_939+36insCC
NM_173483.3:c.939+35_939+36insCC	NP_775754.2:n.939+35_939+36insCC
XM_011527692.1:c.939+35_939+36insCC	XP_011525994.1:n.939+35_939+36insCC
XM_011527693.1:c.939+35_939+36insCC	XP_011525995.1:n.939+35_939+36insCC
XM_011527692.2:c.939+35_939+36insCC	XP_011525994.1:n.939+35_939+36insCC
XM_011527693.2:c.939+35_939+36insCC	XP_011525995.1:n.939+35_939+36insCC
NM_173483.4:c.939+35_939+36insCC MANE Select	NP_775754.2:n.939+35_939+36insCC