Canonical Allele Identifier: CA1940192966
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1847159679

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672240_119672241del , CM000672.2:g.119672240_119672241del GRCh38
NC_000010.10:g.121431752_121431753del , CM000672.1:g.121431752_121431753del GRCh37
NC_000010.9:g.121421742_121421743del NCBI36
NG_016125.1:g.25871_25872del , LRG_742:g.25871_25872del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-15_508-14del MANE Select ENSP00000358081.4:n.508-15_508-14del
ENST00000369085.7:c.508-15_508-14del ENSP00000358081.3:n.508-15_508-14del
ENST00000450186.1:c.334-15_334-14del ENSP00000410036.1:n.334-15_334-14del
NM_004281.3:c.508-15_508-14del , LRG_742t1:c.508-15_508-14del NP_004272.2:n.508-15_508-14del
XM_005270287.1:c.508-15_508-14del XP_005270344.1:n.508-15_508-14del
XM_005270287.2:c.508-15_508-14del XP_005270344.1:n.508-15_508-14del
NM_004281.4:c.508-15_508-14del MANE Select NP_004272.2:n.508-15_508-14del