Canonical Allele Identifier: CA1940190776
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669859A= , CM000672.2:g.119669859A= GRCh38
NC_000010.10:g.121429371A= , CM000672.1:g.121429371A= GRCh37
NC_000010.9:g.121419361A= NCBI36
NG_016125.1:g.23490A= , LRG_742:g.23490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.189A= MANE Select ENSP00000358081.4:p.Pro63=
ENST00000369085.7:c.189A= ENSP00000358081.3:p.Pro63=
ENST00000450186.1:c.15A= ENSP00000410036.1:p.Pro5=
NM_004281.3:c.189A= , LRG_742t1:c.189A= NP_004272.2:p.Pro63=
XM_005270287.1:c.189A= XP_005270344.1:p.Pro63=
XM_005270287.2:c.189A= XP_005270344.1:p.Pro63=
NM_004281.4:c.189A= MANE Select NP_004272.2:p.Pro63=