Canonical Allele Identifier: CA1940191497
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670287_119670288delinsAG , CM000672.2:g.119670287_119670288delinsAG GRCh38
NC_000010.10:g.121429799_121429800delinsAG , CM000672.1:g.121429799_121429800delinsAG GRCh37
NC_000010.9:g.121419789_121419790delinsAG NCBI36
NG_016125.1:g.23918_23919delinsAG , LRG_742:g.23918_23919delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+110_507+111delinsAG MANE Select ENSP00000358081.4:n.507+110_507+111delinsAG
ENST00000369085.7:c.507+110_507+111delinsAG ENSP00000358081.3:n.507+110_507+111delinsAG
ENST00000450186.1:c.333+110_333+111delinsAG ENSP00000410036.1:n.333+110_333+111delinsAG
NM_004281.3:c.507+110_507+111delinsAG , LRG_742t1:c.507+110_507+111delinsAG NP_004272.2:n.507+110_507+111delinsAG
XM_005270287.1:c.507+110_507+111delinsAG XP_005270344.1:n.507+110_507+111delinsAG
XM_005270287.2:c.507+110_507+111delinsAG XP_005270344.1:n.507+110_507+111delinsAG
NM_004281.4:c.507+110_507+111delinsAG MANE Select NP_004272.2:n.507+110_507+111delinsAG