Canonical Allele Identifier: CA305826727
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651562_15651563insCG (hg19) chr19:g.15540751_15540752insCG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540751_15540752insCG , CM000681.2:g.15540751_15540752insCG GRCh38
NC_000019.9:g.15651562_15651563insCG , CM000681.1:g.15651562_15651563insCG GRCh37
NC_000019.8:g.15512562_15512563insCG NCBI36
NG_007987.1:g.37227_37228insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+34_939+35insCG MANE Select ENSP00000269703.1:n.939+34_939+35insCG
ENST00000269703.7:c.939+34_939+35insCG ENSP00000269703.1:n.939+34_939+35insCG
ENST00000601005.2:c.939+34_939+35insCG ENSP00000469866.1:n.939+34_939+35insCG
NM_173483.3:c.939+34_939+35insCG NP_775754.2:n.939+34_939+35insCG
XM_011527692.1:c.939+34_939+35insCG XP_011525994.1:n.939+34_939+35insCG
XM_011527693.1:c.939+34_939+35insCG XP_011525995.1:n.939+34_939+35insCG
XM_011527692.2:c.939+34_939+35insCG XP_011525994.1:n.939+34_939+35insCG
XM_011527693.2:c.939+34_939+35insCG XP_011525995.1:n.939+34_939+35insCG
NM_173483.4:c.939+34_939+35insCG MANE Select NP_775754.2:n.939+34_939+35insCG
Search 100 bp 5'
Search 100 bp 3'