Canonical Allele Identifier: CA1940193050
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672276T= , CM000672.2:g.119672276T= GRCh38
NC_000010.10:g.121431788T= , CM000672.1:g.121431788T= GRCh37
NC_000010.9:g.121421778T= NCBI36
NG_016125.1:g.25907T= , LRG_742:g.25907T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.529T= MANE Select ENSP00000358081.4:p.Ser177=
ENST00000369085.7:c.529T= ENSP00000358081.3:p.Ser177=
ENST00000450186.1:c.355T= ENSP00000410036.1:p.Ser119=
NM_004281.3:c.529T= , LRG_742t1:c.529T= NP_004272.2:p.Ser177=
XM_005270287.1:c.529T= XP_005270344.1:p.Ser177=
XM_005270287.2:c.529T= XP_005270344.1:p.Ser177=
NM_004281.4:c.529T= MANE Select NP_004272.2:p.Ser177=