Canonical Allele Identifier: CA9269773

Gene: CYP4F22

Linked Data

• dbSNP Id: rs376951981
• ExAC: 19:15651568 C / CTGTGA
• MyVariant Identifiers: chr19:g.15651568_15651569insTGTGA (hg19) ; chr19:g.15540757_15540758insTGTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540759_15540760insTGATG , CM000681.2:g.15540759_15540760insTGATG	GRCh38
NC_000019.9:g.15651570_15651571insTGATG , CM000681.1:g.15651570_15651571insTGATG	GRCh37
NC_000019.8:g.15512570_15512571insTGATG	NCBI36
NG_007987.1:g.37235_37236insTGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+42_939+43insTGATG MANE Select	ENSP00000269703.1:n.939+42_939+43insTGATG
ENST00000269703.7:c.939+42_939+43insTGATG	ENSP00000269703.1:n.939+42_939+43insTGATG
ENST00000601005.2:c.939+42_939+43insTGATG	ENSP00000469866.1:n.939+42_939+43insTGATG
NM_173483.3:c.939+42_939+43insTGATG	NP_775754.2:n.939+42_939+43insTGATG
XM_011527692.1:c.939+42_939+43insTGATG	XP_011525994.1:n.939+42_939+43insTGATG
XM_011527693.1:c.939+42_939+43insTGATG	XP_011525995.1:n.939+42_939+43insTGATG
XM_011527692.2:c.939+42_939+43insTGATG	XP_011525994.1:n.939+42_939+43insTGATG
XM_011527693.2:c.939+42_939+43insTGATG	XP_011525995.1:n.939+42_939+43insTGATG
NM_173483.4:c.939+42_939+43insTGATG MANE Select	NP_775754.2:n.939+42_939+43insTGATG