Canonical Allele Identifier: CA1940191392
Gene: BAG3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670206C= , CM000672.2:g.119670206C= GRCh38
NC_000010.10:g.121429718C= , CM000672.1:g.121429718C= GRCh37
NC_000010.9:g.121419708C= NCBI36
NG_016125.1:g.23837C= , LRG_742:g.23837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+29C= MANE Select ENSP00000358081.4:n.507+29C=
ENST00000369085.7:c.507+29C= ENSP00000358081.3:n.507+29C=
ENST00000450186.1:c.333+29C= ENSP00000410036.1:n.333+29C=
NM_004281.3:c.507+29C= , LRG_742t1:c.507+29C= NP_004272.2:n.507+29C=
XM_005270287.1:c.507+29C= XP_005270344.1:n.507+29C=
XM_005270287.2:c.507+29C= XP_005270344.1:n.507+29C=
NM_004281.4:c.507+29C= MANE Select NP_004272.2:n.507+29C=
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