Canonical Allele Identifier: CA1940190991
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669984A= , CM000672.2:g.119669984A= GRCh38
NC_000010.10:g.121429496A= , CM000672.1:g.121429496A= GRCh37
NC_000010.9:g.121419486A= NCBI36
NG_016125.1:g.23615A= , LRG_742:g.23615A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.314A= MANE Select ENSP00000358081.4:p.Asn105=
ENST00000369085.7:c.314A= ENSP00000358081.3:p.Asn105=
ENST00000450186.1:c.140A= ENSP00000410036.1:p.Asn47=
NM_004281.3:c.314A= , LRG_742t1:c.314A= NP_004272.2:p.Asn105=
XM_005270287.1:c.314A= XP_005270344.1:p.Asn105=
XM_005270287.2:c.314A= XP_005270344.1:p.Asn105=
NM_004281.4:c.314A= MANE Select NP_004272.2:p.Asn105=