Canonical Allele Identifier: CA632129604

Gene: CYP4F22

Linked Data

• gnomAD v2: 19-15651559-T-TG
• MyVariant Identifiers: chr19:g.15651560_15651564delinsGCCCGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540748_15540749insG , CM000681.2:g.15540748_15540749insG	GRCh38
NC_000019.9:g.15651559_15651560insG , CM000681.1:g.15651559_15651560insG	GRCh37
NC_000019.8:g.15512559_15512560insG	NCBI36
NG_007987.1:g.37224_37225insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+31_939+32insG MANE Select	ENSP00000269703.1:n.939+31_939+32insG
ENST00000269703.7:c.939+31_939+32insG	ENSP00000269703.1:n.939+31_939+32insG
ENST00000601005.2:c.939+31_939+32insG	ENSP00000469866.1:n.939+31_939+32insG
NM_173483.3:c.939+31_939+32insG	NP_775754.2:n.939+31_939+32insG
XM_011527692.1:c.939+31_939+32insG	XP_011525994.1:n.939+31_939+32insG
XM_011527693.1:c.939+31_939+32insG	XP_011525995.1:n.939+31_939+32insG
XM_011527692.2:c.939+31_939+32insG	XP_011525994.1:n.939+31_939+32insG
XM_011527693.2:c.939+31_939+32insG	XP_011525995.1:n.939+31_939+32insG
NM_173483.4:c.939+31_939+32insG MANE Select	NP_775754.2:n.939+31_939+32insG