Canonical Allele Identifier: CA1940191390
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670203_119670204delinsCT , CM000672.2:g.119670203_119670204delinsCT GRCh38
NC_000010.10:g.121429715_121429716delinsCT , CM000672.1:g.121429715_121429716delinsCT GRCh37
NC_000010.9:g.121419705_121419706delinsCT NCBI36
NG_016125.1:g.23834_23835delinsCT , LRG_742:g.23834_23835delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+26_507+27delinsCT MANE Select ENSP00000358081.4:n.507+26_507+27delinsCT
ENST00000369085.7:c.507+26_507+27delinsCT ENSP00000358081.3:n.507+26_507+27delinsCT
ENST00000450186.1:c.333+26_333+27delinsCT ENSP00000410036.1:n.333+26_333+27delinsCT
NM_004281.3:c.507+26_507+27delinsCT , LRG_742t1:c.507+26_507+27delinsCT NP_004272.2:n.507+26_507+27delinsCT
XM_005270287.1:c.507+26_507+27delinsCT XP_005270344.1:n.507+26_507+27delinsCT
XM_005270287.2:c.507+26_507+27delinsCT XP_005270344.1:n.507+26_507+27delinsCT
NM_004281.4:c.507+26_507+27delinsCT MANE Select NP_004272.2:n.507+26_507+27delinsCT