Canonical Allele Identifier: CA1940193612
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672735T= , CM000672.2:g.119672735T= GRCh38
NC_000010.10:g.121432247T= , CM000672.1:g.121432247T= GRCh37
NC_000010.9:g.121422237T= NCBI36
NG_016125.1:g.26366T= , LRG_742:g.26366T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.909+79T= MANE Select ENSP00000358081.4:n.909+79T=
ENST00000369085.7:c.909+79T= ENSP00000358081.3:n.909+79T=
ENST00000450186.1:c.735+79T= ENSP00000410036.1:n.735+79T=
NM_004281.3:c.909+79T= , LRG_742t1:c.909+79T= NP_004272.2:n.909+79T=
XM_005270287.1:c.909+79T= XP_005270344.1:n.909+79T=
XM_005270287.2:c.909+79T= XP_005270344.1:n.909+79T=
NM_004281.4:c.909+79T= MANE Select NP_004272.2:n.909+79T=