Canonical Allele Identifier: CA1940191329
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670153_119670154delinsGC , CM000672.2:g.119670153_119670154delinsGC GRCh38
NC_000010.10:g.121429665_121429666delinsGC , CM000672.1:g.121429665_121429666delinsGC GRCh37
NC_000010.9:g.121419655_121419656delinsGC NCBI36
NG_016125.1:g.23784_23785delinsGC , LRG_742:g.23784_23785delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.483_484delinsGC MANE Select ENSP00000358081.4:p.Gln161=
ENST00000369085.7:c.483_484delinsGC ENSP00000358081.3:p.Gln161=
ENST00000450186.1:c.309_310delinsGC ENSP00000410036.1:p.Gln103=
NM_004281.3:c.483_484delinsGC , LRG_742t1:c.483_484delinsGC NP_004272.2:p.Gln161=
XM_005270287.1:c.483_484delinsGC XP_005270344.1:p.Gln161=
XM_005270287.2:c.483_484delinsGC XP_005270344.1:p.Gln161=
NM_004281.4:c.483_484delinsGC MANE Select NP_004272.2:p.Gln161=