Canonical Allele Identifier: CA1940196553
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676531G= , CM000672.2:g.119676531G= GRCh38
NC_000010.10:g.121436043G= , CM000672.1:g.121436043G= GRCh37
NC_000010.9:g.121426033G= NCBI36
NG_016125.1:g.30162G= , LRG_742:g.30162G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.977G= MANE Select ENSP00000358081.4:p.Gly326=
ENST00000369085.7:c.977G= ENSP00000358081.3:p.Gly326=
ENST00000450186.1:c.800G= ENSP00000410036.1:p.Gly267=
NM_004281.3:c.977G= , LRG_742t1:c.977G= NP_004272.2:p.Gly326=
XM_005270287.1:c.974G= XP_005270344.1:p.Gly325=
XM_005270287.2:c.974G= XP_005270344.1:p.Gly325=
NM_004281.4:c.977G= MANE Select NP_004272.2:p.Gly326=