Canonical Allele Identifier: CA1940191298
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670143C= , CM000672.2:g.119670143C= GRCh38
NC_000010.10:g.121429655C= , CM000672.1:g.121429655C= GRCh37
NC_000010.9:g.121419645C= NCBI36
NG_016125.1:g.23774C= , LRG_742:g.23774C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.473C= MANE Select ENSP00000358081.4:p.Ala158=
ENST00000369085.7:c.473C= ENSP00000358081.3:p.Ala158=
ENST00000450186.1:c.299C= ENSP00000410036.1:p.Ala100=
NM_004281.3:c.473C= , LRG_742t1:c.473C= NP_004272.2:p.Ala158=
XM_005270287.1:c.473C= XP_005270344.1:p.Ala158=
XM_005270287.2:c.473C= XP_005270344.1:p.Ala158=
NM_004281.4:c.473C= MANE Select NP_004272.2:p.Ala158=