Canonical Allele Identifier: CA632129603

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1468015896
• gnomAD v2: 19-15651557-CCT-C
• MyVariant Identifiers: chr19:g.15651558_15651559del (hg19) ; chr19:g.15540747_15540748del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540748_15540749del , CM000681.2:g.15540748_15540749del	GRCh38
NC_000019.9:g.15651559_15651560del , CM000681.1:g.15651559_15651560del	GRCh37
NC_000019.8:g.15512559_15512560del	NCBI36
NG_007987.1:g.37224_37225del

Transcript Alleles

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