Canonical Allele Identifier: CA378294645

Gene: BAG3

Linked Data

• ClinVar Variation Id: 2581216
• ClinVar RCV Id: RCV003331621
• MyVariant Identifiers: chr10:g.121429388C>T (hg19) ; chr10:g.119669876C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119669876C>T , CM000672.2:g.119669876C>T	GRCh38
NC_000010.10:g.121429388C>T , CM000672.1:g.121429388C>T	GRCh37
NC_000010.9:g.121419378C>T	NCBI36
NG_016125.1:g.23507C>T , LRG_742:g.23507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.206C>T MANE Select	ENSP00000358081.4:p.Pro69Leu
ENST00000369085.7:c.206C>T	ENSP00000358081.3:p.Pro69Leu
ENST00000450186.1:c.32C>T	ENSP00000410036.1:p.Pro11Leu
NM_004281.3:c.206C>T , LRG_742t1:c.206C>T	NP_004272.2:p.Pro69Leu
XM_005270287.1:c.206C>T	XP_005270344.1:p.Pro69Leu
XM_005270287.2:c.206C>T	XP_005270344.1:p.Pro69Leu
NM_004281.4:c.206C>T MANE Select	NP_004272.2:p.Pro69Leu