Canonical Allele Identifier: CA1940196634
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676680C= , CM000672.2:g.119676680C= GRCh38
NC_000010.10:g.121436192C= , CM000672.1:g.121436192C= GRCh37
NC_000010.9:g.121426182C= NCBI36
NG_016125.1:g.30311C= , LRG_742:g.30311C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1126C= MANE Select ENSP00000358081.4:p.Pro376=
ENST00000369085.7:c.1126C= ENSP00000358081.3:p.Pro376=
ENST00000450186.1:c.949C= ENSP00000410036.1:p.Pro317=
NM_004281.3:c.1126C= , LRG_742t1:c.1126C= NP_004272.2:p.Pro376=
XM_005270287.1:c.1123C= XP_005270344.1:p.Pro375=
XM_005270287.2:c.1123C= XP_005270344.1:p.Pro375=
NM_004281.4:c.1126C= MANE Select NP_004272.2:p.Pro376=