Canonical Allele Identifier: CA471634542
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429572T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670060T>A , CM000672.2:g.119670060T>A GRCh38
NC_000010.10:g.121429572T>A , CM000672.1:g.121429572T>A GRCh37
NC_000010.9:g.121419562T>A NCBI36
NG_016125.1:g.23691T>A , LRG_742:g.23691T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.390T>A MANE Select ENSP00000358081.4:p.Ala130=
ENST00000369085.7:c.390T>A ENSP00000358081.3:p.Ala130=
ENST00000450186.1:c.216T>A ENSP00000410036.1:p.Ala72=
NM_004281.3:c.390T>A , LRG_742t1:c.390T>A NP_004272.2:p.Ala130=
XM_005270287.1:c.390T>A XP_005270344.1:p.Ala130=
XM_005270287.2:c.390T>A XP_005270344.1:p.Ala130=
NM_004281.4:c.390T>A MANE Select NP_004272.2:p.Ala130=