Canonical Allele Identifier: CA783646398

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1410320953
• MyVariant Identifiers: chr19:g.15651546_15651555del (hg19) ; chr19:g.15540735_15540744del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540736_15540745del , CM000681.2:g.15540736_15540745del	GRCh38
NC_000019.9:g.15651547_15651556del , CM000681.1:g.15651547_15651556del	GRCh37
NC_000019.8:g.15512547_15512556del	NCBI36
NG_007987.1:g.37212_37221del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+19_939+28del MANE Select	ENSP00000269703.1:n.939+19_939+28del
ENST00000269703.7:c.939+19_939+28del	ENSP00000269703.1:n.939+19_939+28del
ENST00000601005.2:c.939+19_939+28del	ENSP00000469866.1:n.939+19_939+28del
NM_173483.3:c.939+19_939+28del	NP_775754.2:n.939+19_939+28del
XM_011527692.1:c.939+19_939+28del	XP_011525994.1:n.939+19_939+28del
XM_011527693.1:c.939+19_939+28del	XP_011525995.1:n.939+19_939+28del
XM_011527692.2:c.939+19_939+28del	XP_011525994.1:n.939+19_939+28del
XM_011527693.2:c.939+19_939+28del	XP_011525995.1:n.939+19_939+28del
NM_173483.4:c.939+19_939+28del MANE Select	NP_775754.2:n.939+19_939+28del