Canonical Allele Identifier: CA2714101218
Gene: JAZF1 HGNC NCBI

Linked Data

dbSNP Id: rs2128351203

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27936806G>A , CM000669.2:g.27936806G>A GRCh38
NC_000007.13:g.27976425G>A , CM000669.1:g.27976425G>A GRCh37
NC_000007.12:g.27942950G>A NCBI36
NG_011499.1:g.249013C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000283928.10:c.189-41390C>T MANE Select ENSP00000283928.5:n.189-41390C>T
ENST00000649905.1:c.*231-41390C>T ENSP00000497321.1:n.*231-41390C>T
ENST00000283928.9:c.189-41390C>T ENSP00000283928.5:n.189-41390C>T
ENST00000420835.4:n.321-41390C>T
ENST00000427814.5:c.149-41390C>T
ENST00000430432.5:c.90-41390C>T ENSP00000387976.1:n.90-41390C>T
ENST00000447620.5:c.117-41390C>T ENSP00000415096.1:n.117-41390C>T
ENST00000452993.5:c.189-21998C>T ENSP00000415984.1:n.189-21998C>T
ENST00000454041.1:c.189-23353C>T ENSP00000399083.1:n.189-23353C>T
NM_175061.3:c.189-41390C>T NP_778231.2:n.189-41390C>T
XM_006715656.1:c.-66-23353C>T XP_006715719.1:n.-66-23353C>T
XR_926924.1:n.333-23353C>T
NM_175061.4:c.189-41390C>T MANE Select NP_778231.2:n.189-41390C>T