Canonical Allele Identifier: CA1940190829
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669893A= , CM000672.2:g.119669893A= GRCh38
NC_000010.10:g.121429405A= , CM000672.1:g.121429405A= GRCh37
NC_000010.9:g.121419395A= NCBI36
NG_016125.1:g.23524A= , LRG_742:g.23524A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.223A= MANE Select ENSP00000358081.4:p.Arg75=
ENST00000369085.7:c.223A= ENSP00000358081.3:p.Arg75=
ENST00000450186.1:c.49A= ENSP00000410036.1:p.Arg17=
NM_004281.3:c.223A= , LRG_742t1:c.223A= NP_004272.2:p.Arg75=
XM_005270287.1:c.223A= XP_005270344.1:p.Arg75=
XM_005270287.2:c.223A= XP_005270344.1:p.Arg75=
NM_004281.4:c.223A= MANE Select NP_004272.2:p.Arg75=