Canonical Allele Identifier: CA471635011

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1116861
• ClinVar RCV Id: RCV001445417
• dbSNP Id: rs1847240297
• gnomAD v4: 10-119676682-C-T
• MyVariant Identifiers: chr10:g.121436194C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676682C>T , CM000672.2:g.119676682C>T	GRCh38
NC_000010.10:g.121436194C>T , CM000672.1:g.121436194C>T	GRCh37
NC_000010.9:g.121426184C>T	NCBI36
NG_016125.1:g.30313C>T , LRG_742:g.30313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.1128C>T MANE Select	ENSP00000358081.4:p.Pro376=
ENST00000369085.7:c.1128C>T	ENSP00000358081.3:p.Pro376=
ENST00000450186.1:c.951C>T	ENSP00000410036.1:p.Pro317=
NM_004281.3:c.1128C>T , LRG_742t1:c.1128C>T	NP_004272.2:p.Pro376=
XM_005270287.1:c.1125C>T	XP_005270344.1:p.Pro375=
XM_005270287.2:c.1125C>T	XP_005270344.1:p.Pro375=
NM_004281.4:c.1128C>T MANE Select	NP_004272.2:p.Pro376=