Canonical Allele Identifier: CA1940193448
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672528C= , CM000672.2:g.119672528C= GRCh38
NC_000010.10:g.121432040C= , CM000672.1:g.121432040C= GRCh37
NC_000010.9:g.121422030C= NCBI36
NG_016125.1:g.26159C= , LRG_742:g.26159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.781C= MANE Select ENSP00000358081.4:p.Arg261=
ENST00000369085.7:c.781C= ENSP00000358081.3:p.Arg261=
ENST00000450186.1:c.607C= ENSP00000410036.1:p.Arg203=
NM_004281.3:c.781C= , LRG_742t1:c.781C= NP_004272.2:p.Arg261=
XM_005270287.1:c.781C= XP_005270344.1:p.Arg261=
XM_005270287.2:c.781C= XP_005270344.1:p.Arg261=
NM_004281.4:c.781C= MANE Select NP_004272.2:p.Arg261=