Canonical Allele Identifier: CA378294795
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429471C>A (hg19) chr10:g.119669959C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669959C>A , CM000672.2:g.119669959C>A GRCh38
NC_000010.10:g.121429471C>A , CM000672.1:g.121429471C>A GRCh37
NC_000010.9:g.121419461C>A NCBI36
NG_016125.1:g.23590C>A , LRG_742:g.23590C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.289C>A MANE Select ENSP00000358081.4:p.Pro97Thr
ENST00000369085.7:c.289C>A ENSP00000358081.3:p.Pro97Thr
ENST00000450186.1:c.115C>A ENSP00000410036.1:p.Pro39Thr
NM_004281.3:c.289C>A , LRG_742t1:c.289C>A NP_004272.2:p.Pro97Thr
XM_005270287.1:c.289C>A XP_005270344.1:p.Pro97Thr
XM_005270287.2:c.289C>A XP_005270344.1:p.Pro97Thr
NM_004281.4:c.289C>A MANE Select NP_004272.2:p.Pro97Thr
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