Canonical Allele Identifier: CA378294742
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2073229
ClinVar RCV Id: RCV002971722
dbSNP Id: rs1190622666

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669929C>T , CM000672.2:g.119669929C>T GRCh38
NC_000010.10:g.121429441C>T , CM000672.1:g.121429441C>T GRCh37
NC_000010.9:g.121419431C>T NCBI36
NG_016125.1:g.23560C>T , LRG_742:g.23560C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.259C>T MANE Select ENSP00000358081.4:p.Pro87Ser
ENST00000369085.7:c.259C>T ENSP00000358081.3:p.Pro87Ser
ENST00000450186.1:c.85C>T ENSP00000410036.1:p.Pro29Ser
NM_004281.3:c.259C>T , LRG_742t1:c.259C>T NP_004272.2:p.Pro87Ser
XM_005270287.1:c.259C>T XP_005270344.1:p.Pro87Ser
XM_005270287.2:c.259C>T XP_005270344.1:p.Pro87Ser
NM_004281.4:c.259C>T MANE Select NP_004272.2:p.Pro87Ser