Canonical Allele Identifier: CA1940193593
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672675C= , CM000672.2:g.119672675C= GRCh38
NC_000010.10:g.121432187C= , CM000672.1:g.121432187C= GRCh37
NC_000010.9:g.121422177C= NCBI36
NG_016125.1:g.26306C= , LRG_742:g.26306C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.909+19C= MANE Select ENSP00000358081.4:n.909+19C=
ENST00000369085.7:c.909+19C= ENSP00000358081.3:n.909+19C=
ENST00000450186.1:c.735+19C= ENSP00000410036.1:n.735+19C=
NM_004281.3:c.909+19C= , LRG_742t1:c.909+19C= NP_004272.2:n.909+19C=
XM_005270287.1:c.909+19C= XP_005270344.1:n.909+19C=
XM_005270287.2:c.909+19C= XP_005270344.1:n.909+19C=
NM_004281.4:c.909+19C= MANE Select NP_004272.2:n.909+19C=