Canonical Allele Identifier: CA1940191384
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670195T= , CM000672.2:g.119670195T= GRCh38
NC_000010.10:g.121429707T= , CM000672.1:g.121429707T= GRCh37
NC_000010.9:g.121419697T= NCBI36
NG_016125.1:g.23826T= , LRG_742:g.23826T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+18T= MANE Select ENSP00000358081.4:n.507+18T=
ENST00000369085.7:c.507+18T= ENSP00000358081.3:n.507+18T=
ENST00000450186.1:c.333+18T= ENSP00000410036.1:n.333+18T=
NM_004281.3:c.507+18T= , LRG_742t1:c.507+18T= NP_004272.2:n.507+18T=
XM_005270287.1:c.507+18T= XP_005270344.1:n.507+18T=
XM_005270287.2:c.507+18T= XP_005270344.1:n.507+18T=
NM_004281.4:c.507+18T= MANE Select NP_004272.2:n.507+18T=