Canonical Allele Identifier: CA5716283
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2924442
ClinVar RCV Id: RCV003786192
dbSNP Id: rs747274078

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669959C>G , CM000672.2:g.119669959C>G GRCh38
NC_000010.10:g.121429471C>G , CM000672.1:g.121429471C>G GRCh37
NC_000010.9:g.121419461C>G NCBI36
NG_016125.1:g.23590C>G , LRG_742:g.23590C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.289C>G MANE Select ENSP00000358081.4:p.Pro97Ala
ENST00000369085.7:c.289C>G ENSP00000358081.3:p.Pro97Ala
ENST00000450186.1:c.115C>G ENSP00000410036.1:p.Pro39Ala
NM_004281.3:c.289C>G , LRG_742t1:c.289C>G NP_004272.2:p.Pro97Ala
XM_005270287.1:c.289C>G XP_005270344.1:p.Pro97Ala
XM_005270287.2:c.289C>G XP_005270344.1:p.Pro97Ala
NM_004281.4:c.289C>G MANE Select NP_004272.2:p.Pro97Ala