Canonical Allele Identifier: CA378296621

Gene: BAG3

Linked Data

• MyVariant Identifiers: chr10:g.121436157T>G (hg19) ; chr10:g.119676645T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676645T>G , CM000672.2:g.119676645T>G	GRCh38
NC_000010.10:g.121436157T>G , CM000672.1:g.121436157T>G	GRCh37
NC_000010.9:g.121426147T>G	NCBI36
NG_016125.1:g.30276T>G , LRG_742:g.30276T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.1091T>G MANE Select	ENSP00000358081.4:p.Val364Gly
ENST00000369085.7:c.1091T>G	ENSP00000358081.3:p.Val364Gly
ENST00000450186.1:c.914T>G	ENSP00000410036.1:p.Val305Gly
NM_004281.3:c.1091T>G , LRG_742t1:c.1091T>G	NP_004272.2:p.Val364Gly
XM_005270287.1:c.1088T>G	XP_005270344.1:p.Val363Gly
XM_005270287.2:c.1088T>G	XP_005270344.1:p.Val363Gly
NM_004281.4:c.1091T>G MANE Select	NP_004272.2:p.Val364Gly