Canonical Allele Identifier: CA1940190933
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669945G= , CM000672.2:g.119669945G= GRCh38
NC_000010.10:g.121429457G= , CM000672.1:g.121429457G= GRCh37
NC_000010.9:g.121419447G= NCBI36
NG_016125.1:g.23576G= , LRG_742:g.23576G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.275G= MANE Select ENSP00000358081.4:p.Gly92=
ENST00000369085.7:c.275G= ENSP00000358081.3:p.Gly92=
ENST00000450186.1:c.101G= ENSP00000410036.1:p.Gly34=
NM_004281.3:c.275G= , LRG_742t1:c.275G= NP_004272.2:p.Gly92=
XM_005270287.1:c.275G= XP_005270344.1:p.Gly92=
XM_005270287.2:c.275G= XP_005270344.1:p.Gly92=
NM_004281.4:c.275G= MANE Select NP_004272.2:p.Gly92=