Canonical Allele Identifier: CA1940193561
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672636A= , CM000672.2:g.119672636A= GRCh38
NC_000010.10:g.121432148A= , CM000672.1:g.121432148A= GRCh37
NC_000010.9:g.121422138A= NCBI36
NG_016125.1:g.26267A= , LRG_742:g.26267A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.889A= MANE Select ENSP00000358081.4:p.Thr297=
ENST00000369085.7:c.889A= ENSP00000358081.3:p.Thr297=
ENST00000450186.1:c.715A= ENSP00000410036.1:p.Thr239=
NM_004281.3:c.889A= , LRG_742t1:c.889A= NP_004272.2:p.Thr297=
XM_005270287.1:c.889A= XP_005270344.1:p.Thr297=
XM_005270287.2:c.889A= XP_005270344.1:p.Thr297=
NM_004281.4:c.889A= MANE Select NP_004272.2:p.Thr297=