Canonical Allele Identifier: CA1940190607
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669626T= , CM000672.2:g.119669626T= GRCh38
NC_000010.10:g.121429138T= , CM000672.1:g.121429138T= GRCh37
NC_000010.9:g.121419128T= NCBI36
NG_016125.1:g.23257T= , LRG_742:g.23257T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.181-225T= MANE Select ENSP00000358081.4:n.181-225T=
ENST00000369085.7:c.181-225T= ENSP00000358081.3:n.181-225T=
ENST00000450186.1:c.7-225T= ENSP00000410036.1:n.7-225T=
NM_004281.3:c.181-225T= , LRG_742t1:c.181-225T= NP_004272.2:n.181-225T=
XM_005270287.1:c.181-225T= XP_005270344.1:n.181-225T=
XM_005270287.2:c.181-225T= XP_005270344.1:n.181-225T=
NM_004281.4:c.181-225T= MANE Select NP_004272.2:n.181-225T=