Canonical Allele Identifier: CA1940190767
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669853G= , CM000672.2:g.119669853G= GRCh38
NC_000010.10:g.121429365G= , CM000672.1:g.121429365G= GRCh37
NC_000010.9:g.121419355G= NCBI36
NG_016125.1:g.23484G= , LRG_742:g.23484G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.183G= MANE Select ENSP00000358081.4:p.Glu61=
ENST00000369085.7:c.183G= ENSP00000358081.3:p.Glu61=
ENST00000450186.1:c.9G= ENSP00000410036.1:p.Glu3=
NM_004281.3:c.183G= , LRG_742t1:c.183G= NP_004272.2:p.Glu61=
XM_005270287.1:c.183G= XP_005270344.1:p.Glu61=
XM_005270287.2:c.183G= XP_005270344.1:p.Glu61=
NM_004281.4:c.183G= MANE Select NP_004272.2:p.Glu61=