Canonical Allele Identifier: CA1696576028
Gene: JAZF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27937059_27937060delinsAG , CM000669.2:g.27937059_27937060delinsAG GRCh38
NC_000007.13:g.27976678_27976679delinsAG , CM000669.1:g.27976678_27976679delinsAG GRCh37
NC_000007.12:g.27943203_27943204delinsAG NCBI36
NG_011499.1:g.248759_248760delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000283928.10:c.189-41644_189-41643delinsCT MANE Select ENSP00000283928.5:n.189-41644_189-41643delinsCT
ENST00000649905.1:c.*231-41644_*231-41643delinsCT ENSP00000497321.1:n.*231-41644_*231-41643delinsCT
ENST00000283928.9:c.189-41644_189-41643delinsCT ENSP00000283928.5:n.189-41644_189-41643delinsCT
ENST00000420835.4:n.321-41644_321-41643delinsCT
ENST00000427814.5:c.149-41644_149-41643delinsCT
ENST00000430432.5:c.90-41644_90-41643delinsCT ENSP00000387976.1:n.90-41644_90-41643delinsCT
ENST00000447620.5:c.117-41644_117-41643delinsCT ENSP00000415096.1:n.117-41644_117-41643delinsCT
ENST00000452993.5:c.189-22252_189-22251delinsCT ENSP00000415984.1:n.189-22252_189-22251delinsCT
ENST00000454041.1:c.189-23607_189-23606delinsCT ENSP00000399083.1:n.189-23607_189-23606delinsCT
NM_175061.3:c.189-41644_189-41643delinsCT NP_778231.2:n.189-41644_189-41643delinsCT
XM_006715656.1:c.-66-23607_-66-23606delinsCT XP_006715719.1:n.-66-23607_-66-23606delinsCT
XR_926924.1:n.333-23607_333-23606delinsCT
NM_175061.4:c.189-41644_189-41643delinsCT MANE Select NP_778231.2:n.189-41644_189-41643delinsCT