Canonical Allele Identifier: CA1940191129
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670042T= , CM000672.2:g.119670042T= GRCh38
NC_000010.10:g.121429554T= , CM000672.1:g.121429554T= GRCh37
NC_000010.9:g.121419544T= NCBI36
NG_016125.1:g.23673T= , LRG_742:g.23673T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.372T= MANE Select ENSP00000358081.4:p.Thr124=
ENST00000369085.7:c.372T= ENSP00000358081.3:p.Thr124=
ENST00000450186.1:c.198T= ENSP00000410036.1:p.Thr66=
NM_004281.3:c.372T= , LRG_742t1:c.372T= NP_004272.2:p.Thr124=
XM_005270287.1:c.372T= XP_005270344.1:p.Thr124=
XM_005270287.2:c.372T= XP_005270344.1:p.Thr124=
NM_004281.4:c.372T= MANE Select NP_004272.2:p.Thr124=