Canonical Allele Identifier: CA660663636

Gene: BAG3

Linked Data

• dbSNP Id: rs1221338487
• gnomAD v3: 10-119670247-CCT-C
• gnomAD v4: 10-119670247-CCT-C
• MyVariant Identifiers: chr10:g.121429760_121429761del (hg19) ; chr10:g.119670248_119670249del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670249_119670250del , CM000672.2:g.119670249_119670250del	GRCh38
NC_000010.10:g.121429761_121429762del , CM000672.1:g.121429761_121429762del	GRCh37
NC_000010.9:g.121419751_121419752del	NCBI36
NG_016125.1:g.23880_23881del , LRG_742:g.23880_23881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.507+72_507+73del MANE Select	ENSP00000358081.4:n.507+72_507+73del
ENST00000369085.7:c.507+72_507+73del	ENSP00000358081.3:n.507+72_507+73del
ENST00000450186.1:c.333+72_333+73del	ENSP00000410036.1:n.333+72_333+73del
NM_004281.3:c.507+72_507+73del , LRG_742t1:c.507+72_507+73del	NP_004272.2:n.507+72_507+73del
XM_005270287.1:c.507+72_507+73del	XP_005270344.1:n.507+72_507+73del
XM_005270287.2:c.507+72_507+73del	XP_005270344.1:n.507+72_507+73del
NM_004281.4:c.507+72_507+73del MANE Select	NP_004272.2:n.507+72_507+73del