Canonical Allele Identifier: CA1940191411
Gene: BAG3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670216A= , CM000672.2:g.119670216A= GRCh38
NC_000010.10:g.121429728A= , CM000672.1:g.121429728A= GRCh37
NC_000010.9:g.121419718A= NCBI36
NG_016125.1:g.23847A= , LRG_742:g.23847A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+39A= MANE Select ENSP00000358081.4:n.507+39A=
ENST00000369085.7:c.507+39A= ENSP00000358081.3:n.507+39A=
ENST00000450186.1:c.333+39A= ENSP00000410036.1:n.333+39A=
NM_004281.3:c.507+39A= , LRG_742t1:c.507+39A= NP_004272.2:n.507+39A=
XM_005270287.1:c.507+39A= XP_005270344.1:n.507+39A=
XM_005270287.2:c.507+39A= XP_005270344.1:n.507+39A=
NM_004281.4:c.507+39A= MANE Select NP_004272.2:n.507+39A=
Search 100 bp 5'
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