Canonical Allele Identifier: CA1940192965
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672239_119672241delinsCCT , CM000672.2:g.119672239_119672241delinsCCT GRCh38
NC_000010.10:g.121431751_121431753delinsCCT , CM000672.1:g.121431751_121431753delinsCCT GRCh37
NC_000010.9:g.121421741_121421743delinsCCT NCBI36
NG_016125.1:g.25870_25872delinsCCT , LRG_742:g.25870_25872delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-16_508-14delinsCCT MANE Select ENSP00000358081.4:n.508-16_508-14delinsCCT
ENST00000369085.7:c.508-16_508-14delinsCCT ENSP00000358081.3:n.508-16_508-14delinsCCT
ENST00000450186.1:c.334-16_334-14delinsCCT ENSP00000410036.1:n.334-16_334-14delinsCCT
NM_004281.3:c.508-16_508-14delinsCCT , LRG_742t1:c.508-16_508-14delinsCCT NP_004272.2:n.508-16_508-14delinsCCT
XM_005270287.1:c.508-16_508-14delinsCCT XP_005270344.1:n.508-16_508-14delinsCCT
XM_005270287.2:c.508-16_508-14delinsCCT XP_005270344.1:n.508-16_508-14delinsCCT
NM_004281.4:c.508-16_508-14delinsCCT MANE Select NP_004272.2:n.508-16_508-14delinsCCT