Canonical Allele Identifier: CA1940191482
Gene: BAG3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670270G= , CM000672.2:g.119670270G= GRCh38
NC_000010.10:g.121429782G= , CM000672.1:g.121429782G= GRCh37
NC_000010.9:g.121419772G= NCBI36
NG_016125.1:g.23901G= , LRG_742:g.23901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+93G= MANE Select ENSP00000358081.4:n.507+93G=
ENST00000369085.7:c.507+93G= ENSP00000358081.3:n.507+93G=
ENST00000450186.1:c.333+93G= ENSP00000410036.1:n.333+93G=
NM_004281.3:c.507+93G= , LRG_742t1:c.507+93G= NP_004272.2:n.507+93G=
XM_005270287.1:c.507+93G= XP_005270344.1:n.507+93G=
XM_005270287.2:c.507+93G= XP_005270344.1:n.507+93G=
NM_004281.4:c.507+93G= MANE Select NP_004272.2:n.507+93G=
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