Canonical Allele Identifier: CA1940191051
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670002T= , CM000672.2:g.119670002T= GRCh38
NC_000010.10:g.121429514T= , CM000672.1:g.121429514T= GRCh37
NC_000010.9:g.121419504T= NCBI36
NG_016125.1:g.23633T= , LRG_742:g.23633T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.332T= MANE Select ENSP00000358081.4:p.Phe111=
ENST00000369085.7:c.332T= ENSP00000358081.3:p.Phe111=
ENST00000450186.1:c.158T= ENSP00000410036.1:p.Phe53=
NM_004281.3:c.332T= , LRG_742t1:c.332T= NP_004272.2:p.Phe111=
XM_005270287.1:c.332T= XP_005270344.1:p.Phe111=
XM_005270287.2:c.332T= XP_005270344.1:p.Phe111=
NM_004281.4:c.332T= MANE Select NP_004272.2:p.Phe111=