Canonical Allele Identifier: CA9269768
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs778526761
ExAC: 19:15651562 C / CTTG
gnomAD v4: 19-15540751-C-CTTG
MyVariant Identifiers: chr19:g.15651562_15651563insTTG (hg19) chr19:g.15651563delinsTTGG (hg19) chr19:g.15540751_15540752insTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540751_15540752insTTG , CM000681.2:g.15540751_15540752insTTG GRCh38
NC_000019.9:g.15651562_15651563insTTG , CM000681.1:g.15651562_15651563insTTG GRCh37
NC_000019.8:g.15512562_15512563insTTG NCBI36
NG_007987.1:g.37227_37228insTTG

Transcript Alleles

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