Canonical Allele Identifier: CA1696575990
Gene: JAZF1 HGNC NCBI

Linked Data

dbSNP Id: rs1784771671

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27937010T>C , CM000669.2:g.27937010T>C GRCh38
NC_000007.13:g.27976629T>C , CM000669.1:g.27976629T>C GRCh37
NC_000007.12:g.27943154T>C NCBI36
NG_011499.1:g.248809A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000283928.10:c.189-41594A>G MANE Select ENSP00000283928.5:n.189-41594A>G
ENST00000649905.1:c.*231-41594A>G ENSP00000497321.1:n.*231-41594A>G
ENST00000283928.9:c.189-41594A>G ENSP00000283928.5:n.189-41594A>G
ENST00000420835.4:n.321-41594A>G
ENST00000427814.5:c.149-41594A>G
ENST00000430432.5:c.90-41594A>G ENSP00000387976.1:n.90-41594A>G
ENST00000447620.5:c.117-41594A>G ENSP00000415096.1:n.117-41594A>G
ENST00000452993.5:c.189-22202A>G ENSP00000415984.1:n.189-22202A>G
ENST00000454041.1:c.189-23557A>G ENSP00000399083.1:n.189-23557A>G
NM_175061.3:c.189-41594A>G NP_778231.2:n.189-41594A>G
XM_006715656.1:c.-66-23557A>G XP_006715719.1:n.-66-23557A>G
XR_926924.1:n.333-23557A>G
NM_175061.4:c.189-41594A>G MANE Select NP_778231.2:n.189-41594A>G