Canonical Allele Identifier: CA1940196859
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677132G= , CM000672.2:g.119677132G= GRCh38
NC_000010.10:g.121436644G= , CM000672.1:g.121436644G= GRCh37
NC_000010.9:g.121426634G= NCBI36
NG_016125.1:g.30763G= , LRG_742:g.30763G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1578G= MANE Select ENSP00000358081.4:p.Glu526=
ENST00000369085.7:c.1578G= ENSP00000358081.3:p.Glu526=
NM_004281.3:c.1578G= , LRG_742t1:c.1578G= NP_004272.2:p.Glu526=
XM_005270287.1:c.1575G= XP_005270344.1:p.Glu525=
XM_005270287.2:c.1575G= XP_005270344.1:p.Glu525=
NM_004281.4:c.1578G= MANE Select NP_004272.2:p.Glu526=