Canonical Allele Identifier: CA1940191456
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670247_119670249delinsCCT , CM000672.2:g.119670247_119670249delinsCCT GRCh38
NC_000010.10:g.121429759_121429761delinsCCT , CM000672.1:g.121429759_121429761delinsCCT GRCh37
NC_000010.9:g.121419749_121419751delinsCCT NCBI36
NG_016125.1:g.23878_23880delinsCCT , LRG_742:g.23878_23880delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+70_507+72delinsCCT MANE Select ENSP00000358081.4:n.507+70_507+72delinsCCT
ENST00000369085.7:c.507+70_507+72delinsCCT ENSP00000358081.3:n.507+70_507+72delinsCCT
ENST00000450186.1:c.333+70_333+72delinsCCT ENSP00000410036.1:n.333+70_333+72delinsCCT
NM_004281.3:c.507+70_507+72delinsCCT , LRG_742t1:c.507+70_507+72delinsCCT NP_004272.2:n.507+70_507+72delinsCCT
XM_005270287.1:c.507+70_507+72delinsCCT XP_005270344.1:n.507+70_507+72delinsCCT
XM_005270287.2:c.507+70_507+72delinsCCT XP_005270344.1:n.507+70_507+72delinsCCT
NM_004281.4:c.507+70_507+72delinsCCT MANE Select NP_004272.2:n.507+70_507+72delinsCCT