Canonical Allele Identifier: CA1940191369

Gene: BAG3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670184_119670228delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT , CM000672.2:g.119670184_119670228delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	GRCh38
NC_000010.10:g.121429696_121429740delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT , CM000672.1:g.121429696_121429740delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	GRCh37
NC_000010.9:g.121419686_121419730delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	NCBI36
NG_016125.1:g.23815_23859delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT , LRG_742:g.23815_23859delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT MANE Select	ENSP00000358081.4:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGC...
ENST00000369085.7:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	ENSP00000358081.3:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGC...
ENST00000450186.1:c.333+7_333+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	ENSP00000410036.1:n.333+7_333+51delinsAGAGGCCAGGCTCACCAGCCTGC...
NM_004281.3:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT , LRG_742t1:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	NP_004272.2:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGA...
XM_005270287.1:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	XP_005270344.1:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGG...
XM_005270287.2:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT	XP_005270344.1:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGG...
NM_004281.4:c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT MANE Select	NP_004272.2:n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGA...