Canonical Allele Identifier: CA1940190641
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669704A= , CM000672.2:g.119669704A= GRCh38
NC_000010.10:g.121429216A= , CM000672.1:g.121429216A= GRCh37
NC_000010.9:g.121419206A= NCBI36
NG_016125.1:g.23335A= , LRG_742:g.23335A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.181-147A= MANE Select ENSP00000358081.4:n.181-147A=
ENST00000369085.7:c.181-147A= ENSP00000358081.3:n.181-147A=
ENST00000450186.1:c.7-147A= ENSP00000410036.1:n.7-147A=
NM_004281.3:c.181-147A= , LRG_742t1:c.181-147A= NP_004272.2:n.181-147A=
XM_005270287.1:c.181-147A= XP_005270344.1:n.181-147A=
XM_005270287.2:c.181-147A= XP_005270344.1:n.181-147A=
NM_004281.4:c.181-147A= MANE Select NP_004272.2:n.181-147A=