Canonical Allele Identifier: CA1940191134
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670048G= , CM000672.2:g.119670048G= GRCh38
NC_000010.10:g.121429560G= , CM000672.1:g.121429560G= GRCh37
NC_000010.9:g.121419550G= NCBI36
NG_016125.1:g.23679G= , LRG_742:g.23679G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.378G= MANE Select ENSP00000358081.4:p.Ala126=
ENST00000369085.7:c.378G= ENSP00000358081.3:p.Ala126=
ENST00000450186.1:c.204G= ENSP00000410036.1:p.Ala68=
NM_004281.3:c.378G= , LRG_742t1:c.378G= NP_004272.2:p.Ala126=
XM_005270287.1:c.378G= XP_005270344.1:p.Ala126=
XM_005270287.2:c.378G= XP_005270344.1:p.Ala126=
NM_004281.4:c.378G= MANE Select NP_004272.2:p.Ala126=