Canonical Allele Identifier: CA1940196665
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676722G= , CM000672.2:g.119676722G= GRCh38
NC_000010.10:g.121436234G= , CM000672.1:g.121436234G= GRCh37
NC_000010.9:g.121426224G= NCBI36
NG_016125.1:g.30353G= , LRG_742:g.30353G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1168G= MANE Select ENSP00000358081.4:p.Val390=
ENST00000369085.7:c.1168G= ENSP00000358081.3:p.Val390=
NM_004281.3:c.1168G= , LRG_742t1:c.1168G= NP_004272.2:p.Val390=
XM_005270287.1:c.1165G= XP_005270344.1:p.Val389=
XM_005270287.2:c.1165G= XP_005270344.1:p.Val389=
NM_004281.4:c.1168G= MANE Select NP_004272.2:p.Val390=