Canonical Allele Identifier: CA9269754

Gene: CYP4F22

Linked Data

• dbSNP Id: rs775388925
• ExAC: 19:15651551 TGCTGGCCTCCCGAGG / T
• gnomAD v2: 19-15651551-TGCTGGCCTCCCGAGG-T
• gnomAD v4: 19-15540740-TGCTGGCCTCCCGAGG-T
• MyVariant Identifiers: chr19:g.15651552_15651566del (hg19) ; chr19:g.15540741_15540755del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540756_15540770del , CM000681.2:g.15540756_15540770del	GRCh38
NC_000019.9:g.15651567_15651581del , CM000681.1:g.15651567_15651581del	GRCh37
NC_000019.8:g.15512567_15512581del	NCBI36
NG_007987.1:g.37232_37246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+39_939+53del MANE Select	ENSP00000269703.1:n.939+39_939+53del
ENST00000269703.7:c.939+39_939+53del	ENSP00000269703.1:n.939+39_939+53del
ENST00000601005.2:c.939+39_939+53del	ENSP00000469866.1:n.939+39_939+53del
NM_173483.3:c.939+39_939+53del	NP_775754.2:n.939+39_939+53del
XM_011527692.1:c.939+39_939+53del	XP_011525994.1:n.939+39_939+53del
XM_011527693.1:c.939+39_939+53del	XP_011525995.1:n.939+39_939+53del
XM_011527692.2:c.939+39_939+53del	XP_011525994.1:n.939+39_939+53del
XM_011527693.2:c.939+39_939+53del	XP_011525995.1:n.939+39_939+53del
NM_173483.4:c.939+39_939+53del MANE Select	NP_775754.2:n.939+39_939+53del