Canonical Allele Identifier: CA1940193358
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672396A= , CM000672.2:g.119672396A= GRCh38
NC_000010.10:g.121431908A= , CM000672.1:g.121431908A= GRCh37
NC_000010.9:g.121421898A= NCBI36
NG_016125.1:g.26027A= , LRG_742:g.26027A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.649A= MANE Select ENSP00000358081.4:p.Thr217=
ENST00000369085.7:c.649A= ENSP00000358081.3:p.Thr217=
ENST00000450186.1:c.475A= ENSP00000410036.1:p.Thr159=
NM_004281.3:c.649A= , LRG_742t1:c.649A= NP_004272.2:p.Thr217=
XM_005270287.1:c.649A= XP_005270344.1:p.Thr217=
XM_005270287.2:c.649A= XP_005270344.1:p.Thr217=
NM_004281.4:c.649A= MANE Select NP_004272.2:p.Thr217=