Canonical Allele Identifier: CA1940192921
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672206_119672207delinsCA , CM000672.2:g.119672206_119672207delinsCA GRCh38
NC_000010.10:g.121431718_121431719delinsCA , CM000672.1:g.121431718_121431719delinsCA GRCh37
NC_000010.9:g.121421708_121421709delinsCA NCBI36
NG_016125.1:g.25837_25838delinsCA , LRG_742:g.25837_25838delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.508-49_508-48delinsCA MANE Select ENSP00000358081.4:n.508-49_508-48delinsCA
ENST00000369085.7:c.508-49_508-48delinsCA ENSP00000358081.3:n.508-49_508-48delinsCA
ENST00000450186.1:c.334-49_334-48delinsCA ENSP00000410036.1:n.334-49_334-48delinsCA
NM_004281.3:c.508-49_508-48delinsCA , LRG_742t1:c.508-49_508-48delinsCA NP_004272.2:n.508-49_508-48delinsCA
XM_005270287.1:c.508-49_508-48delinsCA XP_005270344.1:n.508-49_508-48delinsCA
XM_005270287.2:c.508-49_508-48delinsCA XP_005270344.1:n.508-49_508-48delinsCA
NM_004281.4:c.508-49_508-48delinsCA MANE Select NP_004272.2:n.508-49_508-48delinsCA