Canonical Allele Identifier: CA1940193130

Gene: BAG3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672304_119672328delinsCCAGCCTGCCTTCCTCCGGCAGGAG , CM000672.2:g.119672304_119672328delinsCCAGCCTGCCTTCCTCCGGCAGGAG	GRCh38
NC_000010.10:g.121431816_121431840delinsCCAGCCTGCCTTCCTCCGGCAGGAG , CM000672.1:g.121431816_121431840delinsCCAGCCTGCCTTCCTCCGGCAGGAG	GRCh37
NC_000010.9:g.121421806_121421830delinsCCAGCCTGCCTTCCTCCGGCAGGAG	NCBI36
NG_016125.1:g.25935_25959delinsCCAGCCTGCCTTCCTCCGGCAGGAG , LRG_742:g.25935_25959delinsCCAGCCTGCCTTCCTCCGGCAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG MANE Select	ENSP00000358081.4:p.Ala186=
ENST00000369085.7:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG	ENSP00000358081.3:p.Ala186=
ENST00000450186.1:c.383_407delinsCCAGCCTGCCTTCCTCCGGCAGGAG	ENSP00000410036.1:p.Ala128=
NM_004281.3:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG , LRG_742t1:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG	NP_004272.2:p.Ala186=
XM_005270287.1:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG	XP_005270344.1:p.Ala186=
XM_005270287.2:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG	XP_005270344.1:p.Ala186=
NM_004281.4:c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG MANE Select	NP_004272.2:p.Ala186=