Canonical Allele Identifier: CA1940190780
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669864C= , CM000672.2:g.119669864C= GRCh38
NC_000010.10:g.121429376C= , CM000672.1:g.121429376C= GRCh37
NC_000010.9:g.121419366C= NCBI36
NG_016125.1:g.23495C= , LRG_742:g.23495C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.194C= MANE Select ENSP00000358081.4:p.Ser65=
ENST00000369085.7:c.194C= ENSP00000358081.3:p.Ser65=
ENST00000450186.1:c.20C= ENSP00000410036.1:p.Ser7=
NM_004281.3:c.194C= , LRG_742t1:c.194C= NP_004272.2:p.Ser65=
XM_005270287.1:c.194C= XP_005270344.1:p.Ser65=
XM_005270287.2:c.194C= XP_005270344.1:p.Ser65=
NM_004281.4:c.194C= MANE Select NP_004272.2:p.Ser65=