Canonical Allele Identifier: CA632129602

Gene: CYP4F22

Linked Data

• dbSNP Id: rs374797305
• gnomAD v2: 19-15651556-G-GACC
• gnomAD v3: 19-15540745-G-GACC
• gnomAD v4: 19-15540745-G-GACC
• MyVariant Identifiers: chr19:g.15651556_15651557insACC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540745_15540746insACC , CM000681.2:g.15540745_15540746insACC	GRCh38
NC_000019.9:g.15651556_15651557insACC , CM000681.1:g.15651556_15651557insACC	GRCh37
NC_000019.8:g.15512556_15512557insACC	NCBI36
NG_007987.1:g.37221_37222insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+28_939+29insACC MANE Select	ENSP00000269703.1:n.939+28_939+29insACC
ENST00000269703.7:c.939+28_939+29insACC	ENSP00000269703.1:n.939+28_939+29insACC
ENST00000601005.2:c.939+28_939+29insACC	ENSP00000469866.1:n.939+28_939+29insACC
NM_173483.3:c.939+28_939+29insACC	NP_775754.2:n.939+28_939+29insACC
XM_011527692.1:c.939+28_939+29insACC	XP_011525994.1:n.939+28_939+29insACC
XM_011527693.1:c.939+28_939+29insACC	XP_011525995.1:n.939+28_939+29insACC
XM_011527692.2:c.939+28_939+29insACC	XP_011525994.1:n.939+28_939+29insACC
XM_011527693.2:c.939+28_939+29insACC	XP_011525995.1:n.939+28_939+29insACC
NM_173483.4:c.939+28_939+29insACC MANE Select	NP_775754.2:n.939+28_939+29insACC