Canonical Allele Identifier: CA1940190980
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669975G= , CM000672.2:g.119669975G= GRCh38
NC_000010.10:g.121429487G= , CM000672.1:g.121429487G= GRCh37
NC_000010.9:g.121419477G= NCBI36
NG_016125.1:g.23606G= , LRG_742:g.23606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.305G= MANE Select ENSP00000358081.4:p.Gly102=
ENST00000369085.7:c.305G= ENSP00000358081.3:p.Gly102=
ENST00000450186.1:c.131G= ENSP00000410036.1:p.Gly44=
NM_004281.3:c.305G= , LRG_742t1:c.305G= NP_004272.2:p.Gly102=
XM_005270287.1:c.305G= XP_005270344.1:p.Gly102=
XM_005270287.2:c.305G= XP_005270344.1:p.Gly102=
NM_004281.4:c.305G= MANE Select NP_004272.2:p.Gly102=