Canonical Allele Identifier: CA1940192891
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672178A= , CM000672.2:g.119672178A= GRCh38
NC_000010.10:g.121431690A= , CM000672.1:g.121431690A= GRCh37
NC_000010.9:g.121421680A= NCBI36
NG_016125.1:g.25809A= , LRG_742:g.25809A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.508-77A= MANE Select ENSP00000358081.4:n.508-77A=
ENST00000369085.7:c.508-77A= ENSP00000358081.3:n.508-77A=
ENST00000450186.1:c.334-77A= ENSP00000410036.1:n.334-77A=
NM_004281.3:c.508-77A= , LRG_742t1:c.508-77A= NP_004272.2:n.508-77A=
XM_005270287.1:c.508-77A= XP_005270344.1:n.508-77A=
XM_005270287.2:c.508-77A= XP_005270344.1:n.508-77A=
NM_004281.4:c.508-77A= MANE Select NP_004272.2:n.508-77A=