Canonical Allele Identifier: CA471634751

Gene: BAG3

Linked Data

• MyVariant Identifiers: chr10:g.121432165T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672653T>G , CM000672.2:g.119672653T>G	GRCh38
NC_000010.10:g.121432165T>G , CM000672.1:g.121432165T>G	GRCh37
NC_000010.9:g.121422155T>G	NCBI36
NG_016125.1:g.26284T>G , LRG_742:g.26284T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.906T>G MANE Select	ENSP00000358081.4:p.Pro302=
ENST00000369085.7:c.906T>G	ENSP00000358081.3:p.Pro302=
ENST00000450186.1:c.732T>G	ENSP00000410036.1:p.Pro244=
NM_004281.3:c.906T>G , LRG_742t1:c.906T>G	NP_004272.2:p.Pro302=
XM_005270287.1:c.906T>G	XP_005270344.1:p.Pro302=
XM_005270287.2:c.906T>G	XP_005270344.1:p.Pro302=
NM_004281.4:c.906T>G MANE Select	NP_004272.2:p.Pro302=