Canonical Allele Identifier: CA1940190688
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669765A= , CM000672.2:g.119669765A= GRCh38
NC_000010.10:g.121429277A= , CM000672.1:g.121429277A= GRCh37
NC_000010.9:g.121419267A= NCBI36
NG_016125.1:g.23396A= , LRG_742:g.23396A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.181-86A= MANE Select ENSP00000358081.4:n.181-86A=
ENST00000369085.7:c.181-86A= ENSP00000358081.3:n.181-86A=
ENST00000450186.1:c.7-86A= ENSP00000410036.1:n.7-86A=
NM_004281.3:c.181-86A= , LRG_742t1:c.181-86A= NP_004272.2:n.181-86A=
XM_005270287.1:c.181-86A= XP_005270344.1:n.181-86A=
XM_005270287.2:c.181-86A= XP_005270344.1:n.181-86A=
NM_004281.4:c.181-86A= MANE Select NP_004272.2:n.181-86A=