Canonical Allele Identifier: CA2611160038
Gene: BAG3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672126_119672132dup , CM000672.2:g.119672126_119672132dup GRCh38
NC_000010.10:g.121431638_121431644dup , CM000672.1:g.121431638_121431644dup GRCh37
NC_000010.9:g.121421628_121421634dup NCBI36
NG_016125.1:g.25757_25763dup , LRG_742:g.25757_25763dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-129_508-123dup MANE Select ENSP00000358081.4:n.508-129_508-123dup
ENST00000369085.7:c.508-129_508-123dup ENSP00000358081.3:n.508-129_508-123dup
ENST00000450186.1:c.334-129_334-123dup ENSP00000410036.1:n.334-129_334-123dup
NM_004281.3:c.508-129_508-123dup , LRG_742t1:c.508-129_508-123dup NP_004272.2:n.508-129_508-123dup
XM_005270287.1:c.508-129_508-123dup XP_005270344.1:n.508-129_508-123dup
XM_005270287.2:c.508-129_508-123dup XP_005270344.1:n.508-129_508-123dup
NM_004281.4:c.508-129_508-123dup MANE Select NP_004272.2:n.508-129_508-123dup