Canonical Allele Identifier: CA471739325
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121436230G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676718G>A , CM000672.2:g.119676718G>A GRCh38
NC_000010.10:g.121436230G>A , CM000672.1:g.121436230G>A GRCh37
NC_000010.9:g.121426220G>A NCBI36
NG_016125.1:g.30349G>A , LRG_742:g.30349G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1164G>A MANE Select ENSP00000358081.4:p.Lys388=
ENST00000369085.7:c.1164G>A ENSP00000358081.3:p.Lys388=
NM_004281.3:c.1164G>A , LRG_742t1:c.1164G>A NP_004272.2:p.Lys388=
XM_005270287.1:c.1161G>A XP_005270344.1:p.Lys387=
XM_005270287.2:c.1161G>A XP_005270344.1:p.Lys387=
NM_004281.4:c.1164G>A MANE Select NP_004272.2:p.Lys388=