Canonical Allele Identifier: CA1940196818
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677047C= , CM000672.2:g.119677047C= GRCh38
NC_000010.10:g.121436559C= , CM000672.1:g.121436559C= GRCh37
NC_000010.9:g.121426549C= NCBI36
NG_016125.1:g.30678C= , LRG_742:g.30678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1493C= MANE Select ENSP00000358081.4:p.Ala498=
ENST00000369085.7:c.1493C= ENSP00000358081.3:p.Ala498=
NM_004281.3:c.1493C= , LRG_742t1:c.1493C= NP_004272.2:p.Ala498=
XM_005270287.1:c.1490C= XP_005270344.1:p.Ala497=
XM_005270287.2:c.1490C= XP_005270344.1:p.Ala497=
NM_004281.4:c.1493C= MANE Select NP_004272.2:p.Ala498=