Canonical Allele Identifier: CA261131
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 39465
dbSNP Id: rs397514507

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676939T>C , CM000672.2:g.119676939T>C GRCh38
NC_000010.10:g.121436451T>C , CM000672.1:g.121436451T>C GRCh37
NC_000010.9:g.121426441T>C NCBI36
NG_016125.1:g.30570T>C , LRG_742:g.30570T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1385T>C MANE Select ENSP00000358081.4:p.Leu462Pro
ENST00000369085.7:c.1385T>C ENSP00000358081.3:p.Leu462Pro
NM_004281.3:c.1385T>C , LRG_742t1:c.1385T>C NP_004272.2:p.Leu462Pro
XM_005270287.1:c.1382T>C XP_005270344.1:p.Leu461Pro
XM_005270287.2:c.1382T>C XP_005270344.1:p.Leu461Pro
NM_004281.4:c.1385T>C MANE Select NP_004272.2:p.Leu462Pro