Canonical Allele Identifier: CA1940196662
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676719A= , CM000672.2:g.119676719A= GRCh38
NC_000010.10:g.121436231A= , CM000672.1:g.121436231A= GRCh37
NC_000010.9:g.121426221A= NCBI36
NG_016125.1:g.30350A= , LRG_742:g.30350A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1165A= MANE Select ENSP00000358081.4:p.Ser389=
ENST00000369085.7:c.1165A= ENSP00000358081.3:p.Ser389=
NM_004281.3:c.1165A= , LRG_742t1:c.1165A= NP_004272.2:p.Ser389=
XM_005270287.1:c.1162A= XP_005270344.1:p.Ser388=
XM_005270287.2:c.1162A= XP_005270344.1:p.Ser388=
NM_004281.4:c.1165A= MANE Select NP_004272.2:p.Ser389=