Canonical Allele Identifier: CA378297176

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1722198
• ClinVar RCV Id: RCV002295222
• MyVariant Identifiers: chr10:g.121436434G>C (hg19) ; chr10:g.119676922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676922G>C , CM000672.2:g.119676922G>C	GRCh38
NC_000010.10:g.121436434G>C , CM000672.1:g.121436434G>C	GRCh37
NC_000010.9:g.121426424G>C	NCBI36
NG_016125.1:g.30553G>C , LRG_742:g.30553G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.1368G>C MANE Select	ENSP00000358081.4:p.Glu456Asp
ENST00000369085.7:c.1368G>C	ENSP00000358081.3:p.Glu456Asp
NM_004281.3:c.1368G>C , LRG_742t1:c.1368G>C	NP_004272.2:p.Glu456Asp
XM_005270287.1:c.1365G>C	XP_005270344.1:p.Glu455Asp
XM_005270287.2:c.1365G>C	XP_005270344.1:p.Glu455Asp
NM_004281.4:c.1368G>C MANE Select	NP_004272.2:p.Glu456Asp